Junior Assistant Manager/ Assistant Manager in M.J. Biopharm Private Limited
Job Posted on Jan 17, 2023
Recruiter Type: | Company |
Company Name: | M.J. Biopharm Private Limited |
Address: | Mumbai, Maharashtra |
Contact Person: | HR |
Email Address: | anuja.bhilare@mjbiopharm.com |
Required in: | Formulation |
Job Department(s): | Research |
Job Title: | Junior Assistant Manager/ Assistant Manager |
Qualification: | M. Pharmacy/ B. Pharmacy/ B.Sc. /M.Sc. |
Job Details: | Biological Injectable formulation development (R&D-Drug Product) Roles and Responsibilities
- Literature survey for Regulated and other markets drug products and other activities for the complete dossier as per regulatory requirement for Formulation Development of new biological injectable formulation.
- Plan and monitor pre-formulation studies for biological products if needed along with innovator products characterization through subordinate scientist.
- Plan and monitor lab trials through subordinate scientist for formulation development of new biological injectable formulation projects as per product development timelines.
- To review analytical data and compile generated during different stages of formulation development of new biological products.
- To plan and execute along with subordinate scientist R & D scale up, plant scale up, Tech transfer batches, exhibit batches and validation batches as tech transfer activities in manufacturing location of new biological injection formulations as per regulatory requirements.
- To coordinate with CMOs (Contract Manufacturing Organization) for planning and executing external Tech transfer activities in manufacturing location of new biological injection formulations as per regulatory requirements.
- Provide technical support to production during execution of commercial validation and for any trouble shooting during production.
- Coordinate and support to Regulatory affairs team regarding product filing, query response and life cycle managements activities.
- Maintain stability record, responsible for stability data compilation and planning.
- Prepare of SOPs, PDR, BMR, MFR, stability protocol, stability report, process optimization protocol and report, TT protocol & Report, PV protocol & report.
- Monitor & maintain the store inventory for API, excipients and packaging material.
- Prepare and maintain of proper batch records, LNBs with all the compilation from F&D and ADL during product development.
- Perform activities related to new product regulatory filing and query response.
- Responsible to maintain good documentation practices, good lab practices and adherence to SOPs in Formulation Development Department.
Desired Candidate Skills:
- Biological Injectable formulation development (Mandatory)
- Literature survey
- Strong knowledge base
- Regulatory requirement
- Pharmaceutical compliance
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Regulatory Exposure: | Not Required |
Experience: | 8+ years |
Vacancies: | 01 |
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