403 Quality Assurance Methodologies jobs in Hyderabad

**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.

Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst to join their team in Hyderabad, Telangana, IN . This critical role involves ensuring the highest standards of quality and compliance for our pharmaceutical products. The ideal candidate will possess a strong scientific background, hands-on experience with analytical techniques, and a thorough understanding of regulatory requirements within the pharmaceutical industry. You will be responsible for performing a wide range of tests, analyzing data, and documenting results to guarantee product safety and efficacy.

Responsibilities:

• Perform routine and advanced analytical testing of raw materials, in-process samples, and finished products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Develop, validate, and transfer analytical methods according to established protocols and regulatory guidelines.
• Analyze test results, interpret data, and prepare accurate and comprehensive reports.
• Investigate out-of-specification (OOS) results and deviations, documenting findings and recommending corrective and preventive actions (CAPA).
• Maintain laboratory equipment, ensuring calibration, qualification, and routine maintenance are performed.
• Ensure adherence to Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and other relevant regulatory standards.
• Prepare and review standard operating procedures (SOPs) for analytical testing and laboratory operations.
• Collaborate with R&D, Manufacturing, and Regulatory Affairs departments to resolve quality issues and support product development.
• Manage laboratory inventory, including chemicals, reagents, and consumables.
• Participate in internal and external audits as required.
• Stay updated with the latest advancements in pharmaceutical analysis and quality control techniques.
• Contribute to continuous improvement initiatives within the Quality Control department.

Qualifications:

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
• Minimum of 3-5 years of experience in pharmaceutical quality control or analytical development.
• Extensive hands-on experience with analytical instrumentation such as HPLC, GC, dissolution testers, and spectrophotometers.
• Proficiency in wet chemistry techniques and compendial testing (USP/EP/BP/IP).
• Strong understanding of GMP, GLP, and ICH guidelines.
• Excellent analytical, problem-solving, and critical thinking skills.
• Meticulous attention to detail and accuracy in data recording and reporting.
• Ability to work independently and as part of a team in a fast-paced laboratory environment.
• Proficient in Microsoft Office Suite and LIMS (Laboratory Information Management System) software.
• Strong written and verbal communication skills.
• Experience with method validation and transfer is highly desirable.

This position requires a dedicated professional who is committed to upholding the highest quality standards in pharmaceutical manufacturing.

Are you a meticulous and experienced Quality Control Engineer passionate about ensuring product excellence? Our client, a leading manufacturing firm at the forefront of innovation, is seeking a Senior Quality Control Engineer to join their esteemed, fully remote team. This role offers an exceptional opportunity to implement robust quality assurance processes, drive continuous improvement, and contribute significantly to the company's reputation for delivering high-quality manufactured goods, all from the convenience of your home office. You will be instrumental in upholding and elevating the company's stringent quality standards.

Responsibilities:

• Develop, implement, and maintain comprehensive quality control systems and procedures throughout the manufacturing lifecycle.
• Conduct rigorous inspections and testing of raw materials, in-process components, and finished products to ensure compliance with specifications.
• Analyze quality data, identify trends, and implement corrective and preventative actions (CAPA) to address deviations.
• Collaborate with engineering, production, and R&D teams to define quality standards and acceptance criteria.
• Lead root cause analysis investigations for quality issues and implement effective solutions.
• Develop and maintain quality documentation, including inspection reports, test procedures, and quality manuals.
• Oversee the calibration and maintenance of quality control equipment and instrumentation.
• Train and mentor junior quality control personnel on quality standards and procedures.
• Stay updated on industry best practices, regulatory requirements, and emerging quality control technologies.
• Conduct internal audits and participate in external supplier audits to ensure quality compliance.
• Contribute to the continuous improvement of manufacturing processes and product quality.
• Ensure all activities are performed in accordance with relevant quality management systems (e.g., ISO 9001).
• Prepare detailed reports on quality performance and present findings to management.

Qualifications:

• Bachelor's degree in Mechanical Engineering, Industrial Engineering, Manufacturing Engineering, or a related technical field.
• Minimum of 5-7 years of progressive experience in quality control or quality assurance within a manufacturing environment.
• Proven expertise in developing and implementing quality control plans and methodologies.
• Strong understanding of statistical process control (SPC), Six Sigma, and Lean Manufacturing principles.
• Experience with various inspection and testing techniques and equipment.
• Proficiency in quality management software and data analysis tools.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong documentation and reporting abilities.
• Effective communication and interpersonal skills, with the capacity to collaborate with cross-functional teams in a remote setting.
• Detail-oriented, methodical, and highly organized.
• Experience in the specific manufacturing sector of our client (e.g., automotive, electronics, consumer goods) is a strong advantage.
• Knowledge of relevant international quality standards.

This position is fully remote , serving manufacturing operations associated with our client's presence in Hyderabad, Telangana, IN . Join our client and lead the charge in ensuring unparalleled product quality.

Our client, a leading pharmaceutical company, is seeking a meticulous and analytical Pharmaceutical Quality Control Analyst to join their team. This critical role ensures that all products meet stringent quality standards and regulatory requirements. The ideal candidate will possess a strong understanding of pharmaceutical testing methodologies, analytical instrumentation, and quality assurance principles. This position is based in **Hyderabad, Telangana, IN**, and requires diligent on-site work.

Key Responsibilities:

• Perform a variety of chemical and physical tests on raw materials, in-process samples, and finished pharmaceutical products.
• Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus.
• Analyze test results, interpret data, and prepare accurate and concise laboratory reports.
• Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines.
• Validate analytical methods and instruments according to established protocols.
• Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective actions.
• Maintain laboratory equipment and ensure calibration is up-to-date.
• Manage inventory of laboratory supplies and reagents.
• Collaborate with other departments, including R&D, production, and regulatory affairs, to resolve quality issues.
• Contribute to the continuous improvement of quality control processes and procedures.

Qualifications:

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
• Minimum of 3-5 years of experience in a pharmaceutical quality control laboratory.
• Hands-on experience with analytical techniques and instrumentation commonly used in pharmaceutical QC.
• Thorough understanding of GMP, GLP, and regulatory requirements (e.g., FDA, EMA).
• Proficiency in data analysis and report writing.
• Excellent attention to detail and problem-solving skills.
• Strong organizational abilities and the capacity to manage multiple tasks.
• Ability to work effectively both independently and as part of a team.

This is an excellent opportunity to contribute to the development and delivery of safe and effective medicines within a reputable organization. If you are committed to quality and possess the required scientific expertise, we encourage you to apply.

Our client is seeking a meticulous and driven Automotive Quality Control Engineer to be based in Hyderabad, Telangana, IN . This pivotal role will involve overseeing and implementing comprehensive quality control procedures throughout the automotive manufacturing and assembly processes. You will be responsible for identifying potential defects, analyzing root causes of quality issues, and developing effective corrective action plans to ensure that all products meet stringent industry standards and customer expectations. Your duties will include conducting regular inspections of components and finished vehicles, performing data analysis, and creating detailed reports on quality performance. A strong understanding of manufacturing processes, quality management systems (such as ISO/TS 16949), and statistical process control (SPC) is essential. The ideal candidate will possess excellent analytical skills, a keen eye for detail, and the ability to work collaboratively with production, engineering, and supply chain teams to drive continuous improvement. You will play a critical role in enhancing product reliability, reducing warranty claims, and upholding the company's reputation for excellence. This position offers a challenging and rewarding environment for an experienced quality professional looking to make a significant impact in the automotive sector. Proactive engagement with suppliers to ensure the quality of incoming materials will also be a key responsibility. You will be instrumental in fostering a quality-centric culture throughout the organization. A proven track record in problem-solving and implementing quality improvement initiatives is required. The successful candidate will be adept at communicating complex technical information clearly and concisely to various stakeholders. This role demands a commitment to maintaining the highest standards of automotive quality.

Quality Control Manager, Customer Support
_corporate_fare_ Google _place_ Gurugram, Haryana, India; Hyderabad, Telangana, India
**Mid**
Experience driving progress, solving problems, and mentoring more junior team members; deeper expertise and applied knowledge within relevant area.
_info_outline_
XNote: By applying to this position you will have an opportunity to share your preferred working location from the following: **Gurugram, Haryana, India; Hyderabad, Telangana, India** .
**Minimum qualifications:**
+ Bachelor's degree in Business, Logistics, Operations, Engineering, a related field, or equivalent practical experience.
+ 5 years of experience managing warehousing and supply chain operations.
+ 5 years of experience working with, supervising, and managing third-party logistics relationships.
**Preferred qualifications:**
+ MBA or Master's degree.
+ Certification in Operations Six Sigma, COPC or LEAN, or other related operations coursework.
+ 5 years of experience analyzing data and generating business insights in order to guide business decisions.
+ Experience in Data center logistics.
+ Knowledge of SQL, expertise in data and insight.
+ Knowledge of digital marketing, programmatic advertising fundamentals.
**About the job**
A problem isn't truly solved until it's solved for all. That's why Googlers build products that help create opportunities for everyone, whether down the street or across the globe. As a Program Manager at Google, you'll lead complex, multi-disciplinary projects from start to finish - working with stakeholders to plan requirements, manage project schedules, identify risks, and communicate clearly with cross-functional partners across the company. Your projects will often span offices, time zones, and hemispheres. It's your job to coordinate the players and keep them up to date on progress and deadlines.
Behind everything our users see online is the architecture built by the Technical Infrastructure team to keep it running. From developing and maintaining our data centers to building the next generation of Google platforms, we make Google's product portfolio possible. We're proud to be our engineers' engineers and love voiding warranties by taking things apart so we can rebuild them. We keep our networks up and running, ensuring our users have the best and fastest experience possible.
**Responsibilities**
+ Set future proof quality processes, frameworks, measures and report outcomes. Track and scale successes, root-cause problems in design/execution and ensure business impact.
+ Process re-engineering to deliver efficiencies and quality outcomes.
+ Drive standardization across delivery regions on process and methods to ensure consistency in experiences, Key Performance Indicators (KPIs) delivery, and leverage economies of scale.
Information collected and processed as part of your Google Careers profile, and any job applications you choose to submit is subject to Google'sApplicant and Candidate Privacy Policy (./privacy-policy) .
Google is proud to be an equal opportunity and affirmative action employer. We are committed to building a workforce that is representative of the users we serve, creating a culture of belonging, and providing an equal employment opportunity regardless of race, creed, color, religion, gender, sexual orientation, gender identity/expression, national origin, disability, age, genetic information, veteran status, marital status, pregnancy or related condition (including breastfeeding), expecting or parents-to-be, criminal histories consistent with legal requirements, or any other basis protected by law. See alsoGoogle's EEO Policy ( ,Know your rights: workplace discrimination is illegal ( ,Belonging at Google ( , andHow we hire ( .
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Google is a global company and, in order to facilitate efficient collaboration and communication globally, English proficiency is a requirement for all roles unless stated otherwise in the job posting.
To all recruitment agencies: Google does not accept agency resumes. Please do not forward resumes to our jobs alias, Google employees, or any other organization location. Google is not responsible for any fees related to unsolicited resumes.
Google is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. See also and If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form:

Our client, a distinguished leader in the automotive manufacturing sector, is seeking a highly experienced Senior Quality Control Engineer to join their manufacturing facility in Hyderabad, Telangana, IN . This critical role ensures that all manufactured products meet stringent quality standards and customer expectations. The ideal candidate will possess a comprehensive understanding of quality management systems, statistical process control (SPC), and various inspection and testing methodologies relevant to the automotive industry. You will be responsible for developing, implementing, and maintaining quality control procedures, conducting root cause analysis for quality defects, and driving continuous improvement initiatives to enhance product reliability and manufacturing efficiency. Key responsibilities include inspecting incoming materials, in-process production, and finished goods; calibrating and maintaining quality control equipment; training production personnel on quality standards; and collaborating with engineering and production teams to resolve quality issues promptly. The successful applicant will have a proven track record in quality assurance within a manufacturing environment, exceptional analytical and problem-solving skills, and strong leadership capabilities. Experience with ISO/TS 16949 or IATF 16949 standards is essential. A bachelor's degree in Mechanical Engineering, Industrial Engineering, or a related technical field is required, along with a minimum of 6 years of experience in quality control engineering, with a significant focus on automotive manufacturing. Strong communication skills and the ability to work effectively under pressure are crucial for this role. If you are dedicated to upholding the highest standards of quality and driving excellence in automotive production, we encourage you to apply.

Our client, a leading provider of specialized cleaning and sanitation services, is seeking a meticulous and experienced Quality Control Manager. This role is vital for ensuring that all services meet the highest standards of hygiene, safety, and client satisfaction. The ideal candidate will have a strong understanding of cleaning protocols, quality assurance processes, and regulatory compliance.

Responsibilities:

• Develop, implement, and maintain quality control standards and procedures for all cleaning and sanitation services.
• Conduct regular inspections and audits of client sites to assess the quality of work and adherence to protocols.
• Identify areas for improvement in service delivery and implement corrective action plans.
• Train and supervise cleaning staff on quality standards, safety procedures, and proper use of equipment and chemicals.
• Monitor compliance with health, safety, and environmental regulations.
• Develop and manage quality assurance documentation, including reports, checklists, and performance metrics.
• Liaise with clients to gather feedback, address concerns, and ensure satisfaction with services provided.
• Investigate customer complaints and implement solutions to prevent recurrence.
• Stay up-to-date with industry best practices, new cleaning technologies, and relevant regulations.
• Manage inventory of cleaning supplies and equipment, ensuring adequate stock levels and proper maintenance.
• Analyze quality data to identify trends and report findings to senior management.
• Foster a culture of quality and continuous improvement among the cleaning team.

Qualifications:

• Bachelor's degree in a relevant field such as Hospitality Management, Environmental Health, or Business Administration.
• Minimum of 5 years of experience in quality control, operations management, or a related role, preferably within the cleaning or facility management industry.
• In-depth knowledge of cleaning and sanitation techniques, chemicals, and equipment.
• Strong understanding of health, safety, and environmental regulations.
• Excellent observational and analytical skills with a keen eye for detail.
• Proven ability to develop and implement quality assurance programs.
• Strong leadership, communication, and interpersonal skills.
• Proficiency in using quality management software and standard office applications.
• Ability to manage multiple tasks and prioritize effectively.
• Experience in conducting training sessions and providing feedback.

This is a hybrid role, requiring the successful candidate to work from our offices in Hyderabad, Telangana, IN and remotely. We are seeking a dedicated professional to uphold our commitment to exceptional cleaning and sanitation standards.

Our client, a renowned pharmaceutical company, is seeking a meticulous and detail-oriented Remote Pharmaceutical Quality Control Analyst to join their vital quality assurance team. This fully remote role allows you to contribute to ensuring the highest standards of quality and compliance in pharmaceutical manufacturing from your home office. You will be responsible for performing various analytical tests, reviewing data, and ensuring that all products meet stringent regulatory requirements and internal specifications.

Key Responsibilities:

• Perform routine analytical testing of raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis spectroscopy).
• Accurately record, review, and document all test results in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Analyze and interpret analytical data, identifying any deviations or out-of-specification (OOS) results.
• Investigate OOS results, conduct root cause analysis, and contribute to corrective and preventative action (CAPA) plans.
• Maintain laboratory equipment, ensure proper calibration, and troubleshoot any instrument issues.
• Prepare and review analytical methods and validation reports.
• Ensure compliance with all relevant regulatory guidelines (e.g., FDA, ICH) and internal quality standards.
• Collaborate with production, R&D, and regulatory affairs teams to resolve quality issues.
• Participate in internal and external audits as needed.

Qualifications:

• Bachelor's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
• Minimum of 2-3 years of experience in pharmaceutical quality control or a related laboratory setting.
• Hands-on experience with common analytical instrumentation (HPLC, GC, dissolution testers) is essential.
• Thorough understanding of GMP, GLP, and relevant regulatory guidelines.
• Strong analytical and problem-solving skills, with a high degree of accuracy and attention to detail.
• Excellent written and verbal communication skills for documentation and reporting.
• Ability to work independently, manage time effectively, and maintain productivity in a remote environment.
• Proficiency in using laboratory information management systems (LIMS) and standard office software.
• This is a fully remote position, ideal for candidates based in or near Hyderabad, Telangana, IN .

This is an excellent opportunity for a dedicated quality professional to contribute to the development and manufacturing of life-saving medicines in a flexible work arrangement.