Job Description
- Ensure testing & release of Finished Products / Raw materials/ Packaging materials as per cGMP in time.
- Approval of analytical method validation protocol, and report.
- Responsible for stability study of all existing products and new projects.
- Facing Internal audits and External Audits and ensure compliance.
- Control of operating expenses.
- Responsible to provide analytical cost of existing/new projects to Accounts.
- Ensure effective implementation of systems and procedures as per GMP, GLP, ISO 9001, ISO 14001 and other regulatory requirements.
- Review of work output and pending work.
- Responsible for Timely data back up of HPLC, GC and storage
- Responsible to maintain & updation of the calculation spreadsheets.
- Responsible to verify and checking of audit trail functioning of the HPLC and GC.
- Carry out OOS investigation along with HOD.
- Ensure effective implementation of SOPs, systems & procedures.
- Ensure entry of data in system.
- Set annual performance goals for Team, monitors performance and guide them to attain it.
- On job training as necessary to develop skills and improve productivity.
- Allocation of work as per the skills of persons & supervision.
- Training to new persons as per Procedure.
- Review of laboratory data.
- To ensure calibration & maintenance of laboratory equipment's.
Qualifications
B.Pharma/ M.Sc
About Us
In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth.
Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices.
Equal employment opportunity
Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics.
We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice.
About The Team
Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited's investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.
Job Info
- Job Identification 4154
- Job Category Quality Control
- Posting Date 06/14/2024, 06:05 AM
- Apply Before 07/31/2024, 06:05 AM
- Degree Level Bachelor's Degree
- Job Schedule Full time
- Locations Piramal Enterprises Limited, Plot # 67-70, Sector II, Dhar, Madhya Pradesh, 454775, IN
