9,314 Quality Manager jobs in India

Roles and Responsibilities  

Experience: 5+
Location: BhiwandiBachelor's degree in a relevant field (e.g., engineering, quality management).
Strong knowledge of quality management systems, quality control tools, and industry-specific regulations.

Desired Candidate Profile  

Perks and Benefits  

Roles and Responsibilities  

Experience: 5+
Location: BhiwandiBachelor's degree in a relevant field (e.g., engineering, quality management).
Strong knowledge of quality management systems, quality control tools, and industry-specific regulations.

Desired Candidate Profile  

Perks and Benefits  

Job description

Key Responsibilities: 

 Will be responsible for managing day to day quality control operations, ensuring compliances
with regulatory requirements and developing strategies for continuous development of quality
control 

Review specifications for products and processes as per FSSAI & IS standards 

 rictly follow requirements for raw material and intermediate products from suppliers and
monitor their compliance 

 sist in maintaining hygiene for the overall plant including personal and Equipment 

 ordinate with the Operations team to identify process correction to eliminate deviation from
quality standards 

 prove the right products or reject defectives 

 intaining documentation for Audit purposes 

 velop, implement, and maintain quality control systems to ensure the consistent production
of high-quality food products

  od understanding of the domain of food safety, RCA and CAPA, quality standards 

 owledge of GMP, GHPANDHACCP 

 suring that all company policies and procedures are followed by all employees 

 erseeing the implementation and maintenance of quality control plans and processes 

 rking with management to develop new quality control processes and procedures 

 sures that quality inspectors are properly trained to carry out of inspections of incoming
materials 

 ke sure that all the quality documents are properly filled, timely checked, verified and
controlled in a manner to be retrieved 

 intain quality levels of products 

 nducting Internal and 3rd party audits

  nitoring the progress of projects to ensure that deadlines are met 

 specting the final output, comparing it to the requirements, and approving or rejecting the
final products 

 suring that quality requirements are met by entities placed under the control of the quality
department 

 oubleshooting 

of key quality concerns with online QC Executives and packaging checkers
 suring best quality of product and minimum customer complaints through stringent on-line
quality control checks and finished product inspection 

Qualifications and Skills: 

 t-graduation degree in Food Science, Food Technology, or a related field 

 oven experience in quality control within the food industry 

 rong understanding of food safety regulations and standards 

 cellent attention to detail and analytical skills 

 fective communication and interpersonal skills 

 ility to work collaboratively in a cross-functional team environment 

 perience of handling team members

  owledge of MS excel and PowerPoint presentation 

 od Communication skill

Apply now-

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Function:**
Quality
**Job Sub** **Function:**
Quality Control
**Job Category:**
People Leader
**All Job Posting Locations:**
Aurangabad, Maharashtra, India
**Job Description:**
SECTION 1: JOB SUMMARY*
- Under the direction of the Director Quality Operations/Site Quality Head, with the objective of
maintaining high quality standards for the product manufacturing process and compliance with
regulatory requirements, administers Quality Control support to the New Products Introduction,
Supply Chain, and directly supervises Quality Control associates and non-exempts in day-to-day
activities supporting manufacturing lines, all in accordance with applicable regulations and
Ethicon written specifications and quality standards.
- Defines India and/or functional strategies and contributes to global strategies for a Quality lab.
Creates and manages multiple complex testing techniques/instruments that result in the
accomplishment of multiple business objectives. Leads the analysis of highly complex issues and
establishes resolutions and or decision points for programs and/or projects. Identifies novel
scenarios and nascent scientific/technical opportunities and seeks to contribute to the
improvement of processes that enable scientists to cultivate new scientific insights.
- Manager QC is responsible for the overall management of the quality laboratory. responsible for driving continuous Quality Excellence, maintaining supply chain compliance, providing franchise support, and communicating internal and external customer facing needs to Site Quality Leaders. This includes support in the delivery of critical initiatives for Medical Device and Supply Chain Quality. In addition, they will identify and facilitate the implementation of key capabilities at the site that will give the Quality team a competitive advantage.
- Plans, coordinates, and direct Quality control activities to ensure continuous production of
products consistent with established quality & regulatory standards by performing the assigned
duties and responsibilities to support manufacturing and timely delivery of product to customers.
SECTION 2: DUTIES & RESPONSIBILITIES*
In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
o Provides Management and Leadership in a laboratory environment.
o Manages laboratory resources to ensure the appropriate level of support and prioritization for
manufacturing activities and timely delivery of products to customers.
o Ensures all laboratory activities are conducted in accordance with government regulations, safety
requirements, Enterprise, Sector and Company policies.
o Ensures the appropriate oversight and guidance for laboratory investigations including reviewing
investigations to ensure that reports are consistent, complete and in alignment with applicable
standards and procedures with appropriate content and references.
o Ensures cGMP compliance in all aspects of the laboratory functions.
o Ensures that all laboratory personnel have the required education and training to perform
assigned job responsibilities.
o Ensures all relevant core competency training modules are deployed to the laboratory personnel
and that all laboratory procedures are aligned with the MD&D and Enterprise Laboratory
Standards.
o Ensures that laboratory equipment and systems are maintained in accordance with procedures
and standards.
o Ensures that validated/verified test methods and qualified and calibrated instruments are used
for quality testing activities.
o provides oversight of Laboratory Instrument Lifecycle and Laboratory Software Lifecycle systems.
o Provides oversight of all Laboratory Quality Systems including Laboratory Change Management activities.
o Provides oversight of Quality Agreements with Contract Laboratories to ensure excellent and appropriate communication between laboratories. Additionally, working with procurement to develop business agreements with Contract Laboratories.
o Ensures Reviewing and approving technical protocols and reports to support validation/verification and qualification activities.
o Ensures monitoring of laboratory metric trends on a regular basis and ensuring that appropriate investigation, corrective actions and/or escalation is conducted as required for recurring trends involving products, methodologies, instrumentation and scientists.
o Provides audit support.
o Leads /sponsors the implementation of improvement initiatives to address recurring laboratory
issues.
o Reviews and approves Quality Records (e.g. non-conformances, CAPA) related to laboratory
events.
o Maintaining knowledge of the regulatory trends related to relevant laboratory testing.
o Communicating and elevating critical business related issues as well as opportunities to senior
management.
o Planning, promoting and organizing required training activities related to different laboratory
testing areas.
o Establishing and maintaining an annual operational budget.
o Monitoring departmental activities to ensure that laboratory personnel follow all company
guidelines related to Health, Safety and Environmental practices. Promoting Good Saves safety
culture.
- For those who supervise or manage a staff, responsible for ensuring that subordinates follow all
Company guidelines related to Health, Safety and Environmental practices and that all resources
needed to do so are available and in good condition, if applicable
o Responsible for ensuring personal and Company compliance with all Federal, State, local and
Company regulations, policies, and procedures
o Performs other duties assigned as needed.
Compliance & Training
- Observes & promotes all regulatory requirements as defined per applicable regulations, rules
& procedures established by the Company, and notified any violation or deviation to the
immediate supervisor or appropriate authority.
- Complies with all training requirements to perform duties of the job.
- Ensure adherence/compliance to Records Management policies and procedures, as
applicable.
Accountability:
- Maintains 5S states of laboratory, GLP & GMP in laboratory.
- Over all Laboratory accountability.
- Team building and credo.
- Laboratory metric & its review.
- Laboratory work as per current procedure and test method.
- Audit readiness within laboratory.
2.1 Authorities:
- Chemical test / Microbiological test Raw Data/Report review and approve (As
applicable)
- Laboratory Log book Review
- Rejection note approval
- Lab Investigation Report, Lab incident approve (As applicable)
- PR/PO approval
- Internal and Cross functional document approval through applicable PLM/ADAPTIV
system
- EtQ (NC , CAPA, audit observation, change request) approval
- OPEX/CAPEX finance related approvals
- Review / Approve Instrument Qualification/calibration/PM/AMC / validations /service
reports/TMV documentation.
- Approve Outward/Inward Gate pass (as applicable)
SECTION 3: EXPERIENCE AND EDUCATION*
- Graduate/Postgraduate/Ph.D in Science degree, preferably in a relevant scientific/technical field/
Pharmaceutical Sciences and 12 or more years of relevant experience in QMS environment. (
OR
- A minimum of 12 years responsibility and experience in a highly regulated environment is
required including a broad and deep working knowledge of the operating functions of quality and
compliance, supply chain, material supply and material handling and control, product
manufacturing and product packaging. Minimum 5 years of experience in Supervisory or
Managerial cadre.An understanding and application of cGMP and internal/external Health
Authority compliance expectations is required.
- Excellent communication, collaboration, and influencing skills across multiple functions and levels
within the organization is required.
- Prior experience with regulatory inspections is desirable.
- Prior experience with project management, Lean, Six Sigma, Operational Excellence, change management training and/or certification is desirable.
SECTION 4: REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and
AFFILIATIONS*
Technical Skills / Behavioral Skills
Functional competencies:
- Understanding of theory, and practical applications, of experimental techniques within a Quality
lab, as well as key processes and activities, and the interdependencies and interactions with other
functions.
- Conducting audits of in-house Quality labs and contract/external Quality labs.
- Technical understanding of, and ability to interpret, applicable regulatory agency regulations and
industry standards.
- Implementing innovative approaches to solving technical problems and troubleshooting, with
limited guidance from management or other scientific personnel, while maintaining a high level of
cGMP awareness.
Professional Competencies
- Operational Excellence: Analytics & Problem Solving, Technology & Data Management, Decision
Making, Knowledge Management.
- Quality & Compliance: Quality Mindset, Compliance Orientation, Environment Health & Safety
- Business Fundamentals: Financial Management & Budgeting, Project Management, Business
Case Development, Business Orientation,
- Business Partnering: Influencing, Change Management, Time Management, Global Mindset &
Management.

Employment Type – Full Time.
Location – Panipat, Haryana.
Experience Required – Minimum 5 years.
Salary – Rs. 40,000/- CTC (Salary is not a bar for deserving candidate)
Working Days – Monday – Saturday.
Roles and Responsibilities:
·   Knowledge on Formulation and Development of Personal Care/Skin Care/Hair
Care/Baby Care/Hygiene Care Cosmetics, Aerosol and Industrial Products in a cost
effective manner within time bound delivery by keeping in view of GMP Norms and
quality.
·   Knowledge of raw materials & packaging materials required to manufacture the above
mentioned products.
·   Should have thorough Knowledge of testing parameters as per required industry
standards for RM/PM/Bulk/Finished Goods.
·   In Process Quality control as per SOP’s & GMP procedures following all the required
norms and compliance as per Drugs and Cosmetics Act.
·   To ensure quality at each level of in process/online, check as per the defined quality
parameters and the customer requirement
·   To ensure the quality of all incoming raw materials, packaging materials, Product
samples, NPD, Bulk and Finished Goods.
·   Should have good knowledge of all the raw materials used in Personal Care, Hygiene
care, Home Care, Skin Care, baby care, cosmetics, aerosol and Industrial products.
·   Control on online inspection of bulk mixing, filling and packing line.
·   Preparation of batch as per formulation.
·   Calibration & Utilization of laboratory instruments.
·   Review of all product related artworks.
·   Handling complete Lab instrument, equipment’s, activities, Lab management &
documentations.
·   Implementing Quality Assurance System & Documentations required in developing
new products.
·   Taking Care of Quality Assurance functions. QA systems implementation,
procedures, documentation.
·   Ensuring QA/ISO implementation. Ensure that legal and statutory as well as quality
requirements at plant location are complied with and data is recorded in the prescribed
manner.
·   Technical support to the Production Team on Products, New Vendor Development
and Packing Trials.
·   Knowledge on product costing.
·   Knowledge on all the Quality related audits.
Skills Required:
·   Qualification: MSC/B-Pharma/M-Pharma
·   Experience – 5 years Plus
·   Industry – Pharma, Cosmetics
·   Salary – Monthly CTC 4000/- (Salary is not a bar for deserving candidate)
·   Location- Panipat, Haryana