Pfizer Dy. Manager in Aurangabad, India

B.Pharm or M.Pharm / M.S.C, with specialization in Pharmaceutics or Industrial Pharmacy and having min. 8- 10 yrs. of experience.

  • Coordinating in training for educating employees on the record management system, storage retention of documents and destruction procedures.

  • Designing the site procedure i.e. SOP, BPR and formats to reduce human error and make it user friendly.

  • Provide training on technical and GDP aspects.

  • Having good knowledge of Data integrity and ALCOA principle.

  • Provide technical support to plant / quality management which defines and implements an effective Data integrity system compliant with the CFR's and meets the business needs of the organization.

  • Execute Gap Assessment of systems, procedures, practices to avoid data integrity issues and GDP errors.

  • Directs, evaluates, and recommends initiatives and policies related to Good Documentation Practices at site.

  • Updation to the team in terms of regulatory expectations related to Data Integrity and Good Documentation Practices.

  • Discussing with the team related to recent regulatory findings for Data Integrity and Good Documentation Practices.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.