4 Job openings found

1 Opening(s)
10.0 Year(s) To 13.0 Year(s)
8.00 LPA TO 14.00 LPA
Role & responsibilities 1. Handling Deviations / Change Control / CAPA / Incidence Reports / Training Records. 2. Handling MFR / BMR / BPR preparation and Review 3. Handling preparation of SOPs / Protocols / QMS. 4. Handling Documentation Control. 5.. Handling of SMF /VMP / Qualification 6. Should be able to handle audit compliance and ...
3 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
QMS: Maintain detailed documentation of QMS(change control, deviation, incident, market complaints, product recall) VMP: maintain and execution of Validation plan as per schedule Master index: Prepare and maintain of Master index for SOP, STP, Protocols, MFR, BMR/BPR Document control: Issue and retrieval of documents like BMR/BPR, SOP, Formats, and log books APQR: Prepare the ...
1 Opening(s)
7.0 Year(s) To 14.0 Year(s)
7.00 LPA TO 16.00 LPA
Education : B. E Chemical Experience: 7-9 yrs. experience in Chemical/ API production Technical skills & Competencies / Language : Know-how of API Production , plant processes and technological updates, SAP Knowledge, data analysis, cGMP & HSE knowhow Behavioral Competencies: Fast, Lean, Inclusive ,Creative, Connected, Responsible KEY ACCOUNTABILITIES Specific Preparing Standard Operating Procedure ( SOP ) ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
The job description is as below: Keep in touch with international legislation, guidelines and customer practices  Keep up to the date with a company’s product range Ensure that a company’s products comply with the current regulations. Coordinate, prepare and review all appropriate documents, for example, dossier and submit them to regulatory authorities within a ...

Drop Your CV

We will consider your Profile for future Jobs

Submit Profile