QA Specialist

Hyderabad, Andhra Pradesh Anicalls (Pty) Ltd

Posted today

Job Viewed

Tap Again To Close

Job Description

• 7 or more years of progressive work experience in business and system testing or equivalent combination of transferrable experience and education.
• Bachelor's degree in an IT-related field or equivalent work experience
• Ability to communicate with the company in business language and with developers in technical language and act as a bridge between them.
• In-depth understanding of the Software Development Life Cycle processes with an emphasis on testing methodologies. Must have in-depth Knowledge of system testing techniques.
• Thorough understanding of the end-to-end business process(s) and flows involved in the system capabilities being tested from the system's under test and end to end.
This advertiser has chosen not to accept applicants from your region.

Data QA Specialist

Hyderabad, Andhra Pradesh YipitData

Posted 9 days ago

Job Viewed

Tap Again To Close

Job Description

About Us:

YipitData is the market-leading data and analytics firm. We analyze billions of data points every day to provide accurate, detailed insights across industries, including consumer brands, technology, software, and healthcare.

Our insights team uses proprietary technology to identify, license, clean, and analyze the data that many of the worlds largest investment funds and corporations depend on. We raised $475M from The Carlyle Group at a valuation over $B, further accelerating our growth and market impact.

We have been recognized multiple times as one of Incs Best Workplaces. As a fast-growing company backed by The Carlyle Group and Norwest Venture Partners, YipitData is driven by a people-first culture rooted in mastery, ownership, and transparency.

With offices in New York, Austin, Miami, Denver, Mountain View, Seattle, Hong Kong, Shanghai, Beijing, Guangzhou, and Singapore, we continue to expand our reach and impact across global markets.

About the Role:

Our newest product offers insights on software companies and is growing rapidly. We are seeking a Financial Analyst (Internal Title: Data QA Specialist) to join our Data Product team in India to manage a large portion of the data cleaning and quality assurance processes for this new product. The Data QA Specialist will be responsible for manually reviewing large datasets of raw financial transaction spend data and helping us transform it into accurate business expense insights. You will verify and make corrections to financial transaction data based on U.S. accounting rules, and youll complete your work primarily using tabular data in our proprietary software. This cleaned data will then be used to build insights products in our fastest-growing initiatives. This position offers the opportunity to meaningfully contribute to the growth of our company. Exceptional employees may have the opportunity to be promoted and manage a team of other Data QA Specialists.

This is a fully remote role based in India.

In general, we expect some overlap with U.S. work hours, and we require greater flexibility (i.e., more overlap) during the first few weeks of training and onboarding. More details on work-hour expectations will be shared during the recruiting process.

We expect hires to start in the position on March 10th, 2025.

As Our Data QA Specialist, You Will:

  • Own manually reviewing and updating raw financial transaction spend data and invoices to help transform it into an accurate representation of business expense insights
  • Verify and make corrections to financial transaction data following U.S. accounting rules, which will include manually adjusting data by:
  • Thoroughly reviewing expense trends over time, across many vendors and different accounting record types
  • Deduplicating overlapping transactions such as vendor bill and journal entries and selecting the correct record
  • Adjusting amortization dates of expenses
  • Inferring amortization dates of expenses, if they are not clear
  • Verifying and tagging the correct vendor for each transaction
  • Document repeated data issues and work with other Data and Engineering teams to improve our data quality assurance processes
  • Primarily complete your work using Google Sheets and our proprietary software
  • Collaborate closely with our U.S.-based Data Product team every day
  • Have the opportunity to be promoted to manage a team of other Data QA Specialists

You Are Likely to Succeed If:

  • You have 0 to 3 years of experience as a data or quality assurance analyst
  • You have at least 1 year of full-time work experience as an A/P bookkeeper, junior accountant, Accounts Payables (A/P) clerk, or in a similar position using U.S. accounting practices
  • You have experience with Netsuite, Sage, Quickbooks, Xero (or similar ERP software)
  • You have exceptional attention to detail
  • You have experience working with large datasets
  • You have experience managing multiple processes in parallel
  • You like to solve problems and puzzles
  • You have excellent written and verbal communication skills, with the ability to interact effectively with vendors and internal teams across time zones and cultures

What We Offer:

Our compensation package includes comprehensive benefits, perks, and a competitive salary:

We care about your personal life and we mean it. We offer flexible vacation, parental leave, team events, learning reimbursement, and more!

Your growth at YipitData is determined by the impact that you are making, not by tenure, unnecessary facetime, or office politics. Everyone at YipitData is empowered to learn, self-improve, and master their skills in an environment focused on ownership, respect, and trust.

The annual salary for this position is anticipated to be 10,000 - 15,000 (USD). The final offer may be determined by a number of factors, including, but not limited to, the applicant's experience, knowledge, skills, and abilities, as well as internal team benchmarks.

We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, marital status, disability, gender, gender identity or expression, or veteran status. We are proud to be an equal opportunity employer.

This advertiser has chosen not to accept applicants from your region.

RCM QA Specialist

Hyderabad, Andhra Pradesh ModMed

Posted today

Job Viewed

Tap Again To Close

Job Description

We are united in our mission to make a positive impact on healthcare. Join Us! 

  • South Florida Business Journal, Best Places to Work 2024
  • Inc. 5000 Fastest-Growing Private Companies in America 2024
  • 2024 Black Book Awards, ranked #1 EHR in 11 Specialties
  • 2024 Spring Digital Health Awards, “Web-based Digital Health” category for EMA Health Records (Gold)
  • 2024 Stevie American Business Award (Silver), New Product and Service: Health Technology Solution (Klara)
  • Who we are:

    We Are Modernizing Medicine (WAMM)! We’re a team of bright, passionate, and positive problem-solvers on a mission to place doctors and patients at the center of care through an intelligent, specialty-specific cloud platform. Our vision is a world where the software we build increases medical practice success and improves patient outcomes. Founded in 2010 by Daniel Cane and Dr. Michael Sherling, we have grown to over 3400 combined direct and contingent team members serving eleven specialties, and we are just getting started! ModMed's global headquarters is based in Boca Raton, FL, with a growing office in Hyderabad, India, and a robust remote workforce across the US, Chile, and Germany.

    The RCM Quality Assurance (QA) Specialist will be responsible for auditing the work of RCM analysts to ensure the highest standards of services are delivered. They will play a pivotal role in identifying process gaps and work closely with onshore and offshore teams to define SOPs and decision trees that will improve the process. 

    The Role:

  • Apply quality assurance expertise by closely monitoring trends, identifying transactions and processes for audits, presenting audit outcomes and recommendations to mitigate gaps to the operations team for resolution.
  • Utilize tools and technologies available to ensure quality concerns are proactively identified and corrected.
  • Work closely with operational teams to resolve process ambiguity by calibrating on audit process and parameters.
  • Ensure Standard Operating Procedures (SOPs) and client specific practice instructions are followed and report any gaps identified with recommendations for improvement. 
  • Continuously improve the quality processes by suggesting innovative ways quality concerns can be quickly identified, fixed and monitored to avoid recurrence.
  • Actively monitor for compliance as per HIPAA guidelines and report any incidence of non-compliance.
  • Actively participate in quality and training huddles, create content, and deliver necessary training to resolve identified skill or knowledge gaps on the team.
  • Audit for adherence to SOPs and other guidelines and provide references and feedback.
  • Review customer feedback/concerns and ensure that corrective action is being taken, adhering to the plan of action.
  • Provide feedback on SOPs so that the processes and procedures are created in such a way that these can be implemented most effectively.
  • Propose changes in decision trees through which inefficiencies and redundancies can be eliminated.
  • Participate and contribute to the success of new clients by identifying any bottlenecks during implementations.
  • Provide training and guidance to team members to improve their knowledge and skills so they are sufficiently equipped to deliver best in class services.
  • Collaborate with the onshore quality team to ensure consistency on processes and procedures being followed across Modmed locations. 
  • Perform additional projects and job duties as assigned.
  • Skills & Requirements:

  • Bachelor's Degree -Bachelor’s preferably in Human Science / Commerce/ Business Administration preferred 
  • Certification in Quality Improvement and Assurance
  • 5+ years of relevant working experience in core Provider RCM out of which minimum 2 years as SME, QA, QA Lead, etc. within a professional setting.
  • Hands-on knowledge of the key functions within RCM is a must.
  • Prior experience of working on Modmed products is a plus. 
  • Experience working on process improvements/ six sigma quality projects preferred. 
  • Proven knowledge of various insurance carriers, including Medicare, private HMOs, PPOs, Capitation and Workers’ Comp. etc.
  • Advanced excel skills such as the ability to use formulas to analyze data, create and format pivot tables and templates, use and conditional formatting and validation functions, able to create visualizations of data through charts, graphs and powerpoint; able to manage information located in multiple software systems.
  • Exceptional written, verbal, and interpersonal communication skills required.
  • Committed to developing expertise in respective ModMed products (PM or gPM) within 3 months of employment.
  • Professional demeanor, team player, strong time management skills required.
  • Able to work during US night shifts within a hybrid work model from home and office is required - this position requires working closely with onshore/offshore teams, as well as with payer reps.
  • ModMed Benefits Highlight: At ModMed, we believe it’s important to offer a competitive benefits package designed to meet the diverse needs of our growing workforce. Eligible Modernizers can enroll in a wide range of benefits:

    India

  • Meals & Snacks: Enjoy complimentary office lunches & dinners on select days and healthy snacks delivered to your desk,
  • Insurance Coverage: Comprehensive health, accidental, and life insurance plans, including coverage for family members, all at no cost to employees,
  • Allowances: Annual wellness allowance to support your well-being and productivity,
  • Earned, casual, and sick leaves to maintain a healthy work-life balance,
  • Bereavement leave for difficult times and extended medical leave options,
  • Paid parental leaves, including maternity, paternity, adoption, surrogacy, and abortion leave,
  • Celebration leave to make your special day even more memorable, and company-paid holidays to recharge and unwind.
  • United States

  • Comprehensive medical, dental, and vision benefits, including a company Health Savings Account contribution,
  • 401(k): ModMed provides a matching contribution each payday of 50% of your contribution deferred on up to 6% of your compensation. After one year of employment with ModMed, 100% of any matching contribution you receive is yours to keep.
  • Generous Paid Time Off and Paid Parental Leave programs,
  • Company paid Life and Disability benefits, Flexible Spending Account, and Employee Assistance Programs,
  • Company-sponsored Business Resource & Special Interest Groups that provide engaged and supportive communities within ModMed,
  • Professional development opportunities, including tuition reimbursement programs and unlimited access to LinkedIn Learning,
  • Global presence and in-person collaboration opportunities; dog-friendly HQ (US), Hybrid office-based roles and remote availability for some roles,
  • Weekly catered breakfast and lunch, treadmill workstations, Zen, and wellness rooms within our BRIC headquarters.
  • PHISHING SCAM WARNING:  ModMed is among several companies recently made aware of a phishing scam involving imposters posing as hiring managers recruiting via email, text and social media. The imposters are creating misleading email accounts, conducting remote "interviews," and making fake job offers in order to collect personal and financial information from unsuspecting individuals. Please be aware that no job offers will be made from ModMed without a formal interview process, and valid communications from our hiring team will come from our employees with a ModMed email address (). Please check senders’ email addresses carefully. Additionally, ModMed will not ask you to purchase equipment or supplies as part of your onboarding process. If you are receiving communications as described above, please report them to the FTC website.

    This advertiser has chosen not to accept applicants from your region.

    QA Specialist - Manual

    Hyderabad, Andhra Pradesh Tech Firefly

    Posted today

    Job Viewed

    Tap Again To Close

    Job Description

    Tech Firefly is teaming up with an American multinational tech company that specializes in Internet services and products. This is a great opportunity for motivated candidates to use their Software Quality Assurance skills for one of the biggest companies in the world.

    We are looking for someone who will specialize in manually testing the web applications. The main focus will be on providing clear and actionable feedback on UI, UX, and responsive design across a variety of platforms (Email Clients and Web Browsers) and languages. QA Specialist will focus on manually testing existing test cases and creating bugs for content creators.

    Hiring Immediately

    • Experience: 2 to 3 years only

    Requirements

    • Bachelor’s degree (technical concentration preferable)
    • 1 to 2 years of Manual QA experience
    • Experience in operating within and leading cross-functional teams (e.g. engineering, product management, sales, implementation)
    • Enjoys working autonomously as well as collaboratively.

    Preferred Qualifications:

    • Experience in Learning Management systems and Web Accessibility
    • Superior problem solving and analytical skills
    • Excellent relationship building, collaboration, strong communication, project management and analytical skills required
    • Able to succeed despite high levels of ambiguity
    • Capable of speaking to both technical and business stakeholders and users

    Benefits

    • American Work Culture & Project Exposure
    • Experience working with one of the best IT companies in the world
    This advertiser has chosen not to accept applicants from your region.

    Salesforce FSL QA Specialist

    Hyderabad, Andhra Pradesh Antal International

    Posted today

    Job Viewed

    Tap Again To Close

    Job Description

    Job Description

    Roles & Responsibilities

  • Develop and execute test strategies for Salesforce FSL implementations.
  • Perform functional, regression, and integration testing for FSL applications (desktop + mobile).
  • Validate FSL scheduling, service territories, work orders, and dispatch console workflows.
  • Collaborate with developers and consultants to resolve defects.
  • Automate regression test cases where applicable.
  • Qualifications

  • Bachelor’s in IT/Engineering or related field.
  • 3–6 years of QA experience, with 2+ years testing Salesforce/FSL projects.
  • Strong knowledge of Salesforce testing methodologies and tools.
  • Experience with API testing (Postman, SOAPUI) and test automation (Selenium, Provar, or Tosca).
  • Familiarity with Agile/Scrum.
  • Experience: 7+ Years

    Location: Hyderabad

    Working mode: Hybrid, 3 days in a week

    Check Your Resume for Match

    Upload your resume and our tool will compare it to the requirements for this job like recruiters do.

    This advertiser has chosen not to accept applicants from your region.

    QA Lead Specialist

    Hyderabad, Andhra Pradesh beBeeQuality

    Posted today

    Job Viewed

    Tap Again To Close

    Job Description

    We are seeking an experienced Quality Assurance Consultant to oversee quality checks for product batches before export. This role involves close coordination with accredited labs, suppliers and internal teams to ensure compliance with quality standards and regulatory requirements.

    Key Responsibilities:

    • Coordinate with NABL-accredited laboratories for COA, HPTLC, heavy metals and microbial testing.
    • Review supplier GMP compliance, batch manufacturing records and packaging quality.
    • Maintain and update QA checklists for each batch.
    • Approve and release batches for shipment after quality clearance.
    • Provide ongoing support for audits and export documentation as needed.

    Requirements:

    • Minimum 4+ years of experience in Quality Assurance within pharma, Ayurveda or related industries.
    • Strong knowledge of COA interpretation, testing methodologies and lab coordination.
    • Familiarity with GMP standards and export QA processes.
    • Ability to coordinate remotely with suppliers, labs and regulatory bodies.

    Our Ideal Candidate

    • The ideal candidate will have a proven track record of ensuring quality standards are met across multiple locations.
    • A strong analytical mindset with excellent problem-solving skills is essential for this role.

    About the Role

    This is a fantastic opportunity for a talented professional looking to make a real impact in our organization. If you are passionate about delivering high-quality products and services, we encourage you to apply.

    This advertiser has chosen not to accept applicants from your region.

    Specialist QA

    Hyderabad, Andhra Pradesh Amgen

    Posted today

    Job Viewed

    Tap Again To Close

    Job Description

    **AIN Specialist QA - Job Description**
    **Join Amgen's Mission of Serving Patients**
    At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
    Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
    Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
    **Position Summary:**
    The AIN Specialist QA plays a critical role in supporting product disposition related tasks across the Amgen Quality Operations Network. The Specialist QA will leverage industry, technical, and quality systems knowledge to provide support of product expiry management processes, product complaints processes, disposition manager training, and fulfillment of disposition related data requests across the network. The position will be responsible for tasks including the key responsibilities documented below and other disposition related job functions.
    This candidate will primarily work during regular working hours (9 am - 6 PM local time) to enable the business in delivering Amgen's mission to serve patients and may lead a shift-based team that provides coverage in support of the Amgen network across multiple time zones. The candidate may need to work outside of his/her routine workday to support business needs and will be responsible for determining the same for their staff. The individual will be required to work from our office located in Hyderabad India (Amgen India-AIN). The candidate will also lead the remote support from AIN to Amgen sites across multiple time zones globally.
    **Key Responsibilities**
    **DSI/DS/DP material shelf-life extension**
    - Executing the GMP process to extend expiration dates for clinical and commercial products produced at Amgen.
    - Updating batch product expiration dates in the Amgen SAP inventory management system.
    - Evaluating (approve or reject) expiry-SAF forms (expiry stability assessment forms).
    **Disposition Support of Partner Requests**
    - Support requests made by Amgen partners for data and information related to their partnered product batches manufactured at Amgen sites.
    - Data recovery from systems including, but not limited to, manufacturing execution system electronic batch records, the quality control laboratory information system, the regulatory information management system, and the Amgen enterprise resource management system (SAP).
    - Uploading and communication of collected data to Amgen partners.
    **COA Generation, special requests after disposition**
    - Generation and provision of Certificate of Analysis (CofA) records for Amgen drug substance, drug product, or final drug product batches.
    - Uploading and communication of collected documentation to requestor (i.e. Amgen partners, regulatory compliance to support RTQs, process development).
    **Disposition Manager Training**
    - Execution and delivery of quality systems training to new disposition managers across the Amgen network via virtual meetings.
    - Training subject matter to include use of quality systems applied to execute the disposition process (i.e. ERP/SAP, MES/EBR, ARRS, LIMS, TW, CDOCS, DQMS, Kneat, etc.)
    - Maintenance and revision of training document materials in the controlled documents management system (CDOCs).
    **Product Complaints**
    - Execution of the drug substance, drug product, and final drug product complaint full batch record review process.
    - Assessing electronic batch record (EBRs) documentation in the manufacturing execution system (MES) to identify any potential issues relevant to the complaint.
    - Recording the results of the complaints batch record assessment in the Bioconnect quality system.
    **Preferred Qualifications**
    - Experience in project management and related systems
    - Proficiency in technical writing and data visualization tools; experience with Smartsheet, Tableau, or equivalent platforms preferred.
    - Excellent verbal and written communication skills
    - Proven ability to lead and collaborate within cross-functional teams in a dynamic, fast-paced setting.
    - Experience in manufacturing environments
    **Core Competencies**
    - Experience working in a regulated environment with knowledge of Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) requirements.
    - Experience working with Quality Systems that may include enterprise resource planning (ERP/SAP), regulatory information management (RIM), controlled document management (CDOCS), change control (QMTS), deviation (DQMS), and quality control laboratory information management systems (LIMS).
    -Experienced in staff training and development.
    - Technical Document Drafting and Workflow Ownership
    Basic Qualifications and Experience:
    - Master's degree with 8-12 years of Pharma and Biotech commercial or clinical manufacturing Quality experience.
    This advertiser has chosen not to accept applicants from your region.
    Be The First To Know

    About the latest Quality assurance measures Jobs in Hyderabad !

    Quality Control Engineer

    500001 Hyderabad, Andhra Pradesh ₹60000 Annually WhatJobs

    Posted 9 days ago

    Job Viewed

    Tap Again To Close

    Job Description

    full-time
    Our client is seeking a meticulous and experienced Quality Control Engineer to join their manufacturing facility in Hyderabad, Telangana, IN . This role is integral to ensuring that all manufactured products meet the highest standards of quality and reliability. The successful candidate will be responsible for developing, implementing, and maintaining quality control systems and procedures throughout the production process. You will conduct inspections and tests on raw materials, in-process components, and finished goods to identify defects and ensure compliance with specifications. This role requires a deep understanding of manufacturing processes, quality assurance methodologies, and statistical process control (SPC). You will work closely with production teams, engineering, and suppliers to address quality issues, implement corrective and preventive actions (CAPA), and drive continuous improvement in product quality. Key responsibilities include developing and maintaining quality documentation, conducting root cause analysis for quality failures, and participating in internal and external audits. The Quality Control Engineer will also be involved in process validation, supplier quality management, and the implementation of quality management systems such as ISO 9001. This position demands strong analytical skills, attention to detail, and the ability to interpret technical specifications and standards. If you are a quality-focused professional looking to make a significant contribution to a reputable manufacturing organization, we invite you to apply.

    Key Responsibilities:
    • Develop, implement, and maintain quality control plans and procedures.
    • Conduct inspections and tests on materials, components, and finished products.
    • Analyze quality data and identify trends, defects, and areas for improvement.
    • Perform root cause analysis for quality issues and implement effective corrective and preventive actions (CAPA).
    • Collaborate with production and engineering teams to resolve quality-related problems.
    • Ensure compliance with industry standards, regulatory requirements, and customer specifications.
    • Manage supplier quality, including audits and performance evaluations.
    • Develop and maintain quality documentation, including test reports and quality manuals.
    • Participate in internal and external audits of the quality management system.
    • Promote a culture of quality and continuous improvement throughout the organization.

    Qualifications:
    • Bachelor's degree in Engineering (Mechanical, Electrical, or related field) or a relevant technical discipline.
    • 3-5 years of experience in quality control or quality assurance within a manufacturing environment.
    • Strong knowledge of quality management systems (e.g., ISO 9001) and statistical process control (SPC).
    • Experience with root cause analysis tools and techniques (e.g., 5 Whys, Fishbone diagrams).
    • Proficiency in interpreting technical drawings, specifications, and test methods.
    • Excellent analytical, problem-solving, and organizational skills.
    • Strong communication and interpersonal skills to effectively collaborate with teams.
    • Detail-oriented with a commitment to accuracy.
    • Experience with metrology and calibration procedures is a plus.
    This advertiser has chosen not to accept applicants from your region.

    Senior Manager Quality Control

    Hyderabad, Andhra Pradesh Amgen

    Posted today

    Job Viewed

    Tap Again To Close

    Job Description

    **ABOUT AMGEN**
    Amgen harnesses the best of biology and technology to fight the world's toughest diseases, and make people's lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what's known today.
    **ABOUT THE ROLE**
    **Role Description:**
    In this vital role, you will lead the Amgen India, Quality Control Technical Resources Team. This is a unique opportunity to support the global Quality Control network and to learn about the testing of Amgen products through various stages of the product lifecycle. In addition, as this is a newly formed team, the Senior Manager will have the opportunity to develop new business processes and to strategically develop the team structure.
    The QC Technical Resources team will primarily provide centralized document management support for the global QC Network. This will include the creation and/or revision of controlled documents within Amgen's enterprise document management system for a variety of QC processes. The Senior Manager Quality Control will provide management oversight of this team while fostering a culture of innovation, quality and collaboration. The Senior Manager will report directly to Amgen India Quality Leadership.
    This candidate will primarily work during regular working hours (9 AM - 6 PM local time) to enable the business in delivering Amgen's mission to serve patients and may lead a shift-based team that provides coverage in support of the Amgen network across multiple time zones. The candidate may need to work outside of his/her routine workday to support business needs and will be responsible for determining the same for their staff. The individual will be required to work from our office located in Hyderabad India (Amgen India-AIN). The candidate will also lead the remote support from AIN to Amgen sites across multiple time zones globally.
    **Roles & Responsibilities:**
    The Senior Manager Quality Control will be accountable for the following activities:
    - Daily management of the Quality Control Technical Resources team
    - Responsible for organizing team resources to ensure that agreed upon due dates are met for QC Network requests
    - Responsible for creating and maintaining business processes and tools that will facilitate the management and visibility of QC network requests
    - Responsible for ensuring that the Technical Resources team has access to the required laboratory information management and enterprise systems needed to carry out document management tasks (for example, LIMS, electronic laboratory notebook).
    - Responsible for leading issue resolution and problem-solving exercises within the team and cross-functionally, as needed
    - Support staff training, career development and performance management
    - Responsible for ensuring compliance with safety guidelines, cGMPs and other applicable regulatory requirements.
    **Additional Responsibilities:**
    - Participate in Amgen global network teams
    - Establish and enable LEAN principles across area of responsibility
    - Establish and enable department goals, strategies and KPIs
    - Champion site and QC global process improvements
    - Interfaces with management on significant matters, often requiring the coordination of activity across organizational units
    - Plans and organizes project assignments of substantial variety and complexity
    - Translates complex data into actionable information and applies strong technical knowledge to meet business objectives
    - Identifies process gaps, introduces innovative solutions, and leads operational excellence projects to improve efficiency and productivity, while decreasing expense/operating costs.
    - Leads root cause analysis discussions for more complex problems to develop and efficiently implement effective permanent solutions.
    **Basic Qualifications and Experience:**
    + Master's degree with 12-16 years of Pharma and Biotech commercial or clinical manufacturing Quality Control experience
    AND
    + 5 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources
    **Functional Skills:**
    **Must-Have Skills:**
    + Experience working and leading teams in a cGMP laboratory environment.
    + Strong technical writing skills within a highly regulated environment.
    + Working knowledge of cGMP regulations, practices, and trends pertaining to Quality Control.
    + Experience managing staff and/or leading teams, projects, programs or directing the allocation of resources.
    **Good-to-Have Skills:**
    + Track record of building or participating as a member of high performing team.
    + Experience with various laboratory computer systems and applications.
    + Strong leadership and negotiation skills with a demonstrated ability to influence different styles.
    + Demonstrated innovative thinking and ability to transform work organizations.
    + Exposure to Operational Excellence initiatives.
    + Understanding of quality management systems and quality control processes related to drug substance and drug product for clinical and commercial operations.
    + Demonstrated ability to navigate through ambiguity and provide structured problem solving.
    + Demonstrated ability to coordinate multi-functional project teams and deliver on schedule.
    + Demonstrated ability to coordinate and lead cross-functional teams.
    + Demonstrated ability to find opportunities and implement new technologies and services to transform the business into a more agile, efficient and effective organization.
    + Demonstrated skills in staff motivation, coaching/mentoring and professional development.
    + Great teammate who can collaborate and provide leadership through influence to achieve the required results.
    **EQUAL OPPORTUNITY STATEMENT**
    Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
    We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.
    This advertiser has chosen not to accept applicants from your region.
     

    Nearby Locations

    Other Jobs Near Me

    Industry

    1. request_quote Accounting
    2. work Administrative
    3. eco Agriculture Forestry
    4. smart_toy AI & Emerging Technologies
    5. school Apprenticeships & Trainee
    6. apartment Architecture
    7. palette Arts & Entertainment
    8. directions_car Automotive
    9. flight_takeoff Aviation
    10. account_balance Banking & Finance
    11. local_florist Beauty & Wellness
    12. restaurant Catering
    13. volunteer_activism Charity & Voluntary
    14. science Chemical Engineering
    15. child_friendly Childcare
    16. foundation Civil Engineering
    17. clean_hands Cleaning & Sanitation
    18. diversity_3 Community & Social Care
    19. construction Construction
    20. brush Creative & Digital
    21. currency_bitcoin Crypto & Blockchain
    22. support_agent Customer Service & Helpdesk
    23. medical_services Dental
    24. medical_services Driving & Transport
    25. medical_services E Commerce & Social Media
    26. school Education & Teaching
    27. electrical_services Electrical Engineering
    28. bolt Energy
    29. local_mall Fmcg
    30. gavel Government & Non Profit
    31. emoji_events Graduate
    32. health_and_safety Healthcare
    33. beach_access Hospitality & Tourism
    34. groups Human Resources
    35. precision_manufacturing Industrial Engineering
    36. security Information Security
    37. handyman Installation & Maintenance
    38. policy Insurance
    39. code IT & Software
    40. gavel Legal
    41. sports_soccer Leisure & Sports
    42. inventory_2 Logistics & Warehousing
    43. supervisor_account Management
    44. supervisor_account Management Consultancy
    45. supervisor_account Manufacturing & Production
    46. campaign Marketing
    47. build Mechanical Engineering
    48. perm_media Media & PR
    49. local_hospital Medical
    50. local_hospital Military & Public Safety
    51. local_hospital Mining
    52. medical_services Nursing
    53. local_gas_station Oil & Gas
    54. biotech Pharmaceutical
    55. checklist_rtl Project Management
    56. shopping_bag Purchasing
    57. home_work Real Estate
    58. person_search Recruitment Consultancy
    59. store Retail
    60. point_of_sale Sales
    61. science Scientific Research & Development
    62. wifi Telecoms
    63. psychology Therapy
    64. pets Veterinary
    View All Quality Assurance Measures Jobs View All Jobs in Hyderabad