Johnson & Johnson Hiring Sr. Officer Make Q&C M. Pharm/ B. Pharm/ M. Sc. Apply Now
Purpose of the position:
Ensure compliance to the requirements of applicable Good
Manufacturing Practices (Schedule M, U of D&C Act, FSSAI. Legal Metrology
etc) in all manufacturing workshops (Band-Aid, Baby Powder, Food – ORSL Base
kit & Sanitary Napkins) of the plant.
Governance to the requirements of Good Laboratory Practices
(Schedule L-I of D&C Act) in the Quality Control Laboratory, enabling
timely & accurate disposition for incoming materials, intermediates, bulk
& finished products manufactured at the plant.
Ensure compliance to the Regulatory Compliance at the site.
General Responsibilities:
1. Responsible for
effective deployment of Quality System elements viz., investigations of
Non-conformances/Deviations & Market Complaints, change management, CAPA
management, Training program, Internal Audit program, etc. to drive on time and
effective closures of the actions identified.
2. Responsible for review of Batch Manufacturing Record and
other applicable GxP documents and act as authorized personal for production
batch release.
3. Responsible for coordinating with suppliers for the
investigations related to material issues during production and ensure the
closure of the same in the given timelines.
4. Conduct GMP rounds and ensure quality culture management
at shop floor
5. Responsible for governance of timely line clearance,
in-process checks and sampling.
6. Ensure Stability management by conducting MPS studies,
etc.
7. Conduct trainings on the revised procedures/BMR and drive
effectiveness.
8. Ensure closure of observations related to internal and
external audit and coordinate with respective stakeholders for timely closure
of AAPs.
9.Lead the projects identified in JJPS Projects and support
to CIP/Improvement Projects.
10. Responsible for execution of activities allocated by
supervisor on timely basis.
11. Preparation of Trend data of Sanpro, Band Aid and Powder
for Complaints.
12.Responsibe for preparation of Annual Product Review,
wherever applicable.
Qualifications:
Technical Qualification
. Education: M. Pharm/ B. Pharm/ M. Sc. from reputed
university.
Sound knowledge of GMP, GLP and Local Regulations (Drugs
& Cosmetics Act of India,
Bureau of Indian Standards, ISO 9001 etc.)
. Experience: Having around 3-4 years of experience in
Quality Control and Quality Assurance function of Chemical and Pharmaceutical
Industry.
Skills
Computer Literacy: Good working Knowledge of MS office.
Good communication & interpersonal skills, flair for
quality, team player, quick learner.
Able to take added responsibilities.
Keen to learn and improve skills.
Proactive risk assessment approach
TO APPLY CLICK HERE
FOR JOB UPDATES
JOIN IN GROUP FOR DAILY UPDATES
No comments:
Post a Comment