Milan Laboratories (India) Pvt. Ltd. leading Pharmaceutical Manufacturer and Exporter from India. An ISO 9001:2015, WHO, cGMP, USFDA, EUGMP, UNICEF & UK-MHRA-certified company, is a Govt. Recognized Star Export House and a winner of various awards for Quality Excellence and Outstanding Export Performance.
Dear Job aspirants,
We are currently looking for a motivated and experienced individual to fill this important role in our organization. We are conducting a walk-in interview on 02 April 2023, at Hotel Ginger, Baruch for the department of Quality Assurance – Injectables (SVP) & Oral Solid Dosage (OSD) Plants.
If you are passionate about your work and are looking for an opportunity to grow in your career, then this is the right platform for you.
Position Details:
Injectables (SVP)
- Officer/Sr. Officer – 3 ( Experience 1 – 4 yrs)
- Officer/Sr. Officer-IPQA – 3 ( Experience 1 – 4 yrs)
- Sr. Officer/Executive – 3 ( Experience 3 – 7 yrs)
- Sr. Officer/Executive-LAB – 1 ( Experience 3 – 7 yrs)
- Manager/ Asst. Manager – 1 ( Experience 12 – 18 yrs)
Oral Solid Dosage (OSD)
- Officer – QA/IPQA – 6 ( Experience 1 – 2 yrs)
- Officer/Sr. Officer QAMS – 3 ( Experience 1 – 4 yrs)
Requirements:
- Minimum educational qualification: B.Pharm / M.Pharm.
- Prior experience is required.
- Knowledge of cGMP, safety regulations, and quality standards.
- Ability to work in a team and communicate effectively.
- Willingness to work in shifts.
Job Description:
1. Review of qualification and validation documents (URS, DQ, FAT/SAT, IQ, OQ).
2. Participation in Qualification and validation activities and compilation of qualification and validation records.
3. Preparation and compilation of Qualification and validation report.
4. Preparation of SOP.
5. Maintaining the Hard copies. Ensuring timely approval of the above documents by stake holders and maintaining the same.
6. Supervision/execution of the qualification and validation activity protocol along with vendor.
7. Participation in SAT, IQ and OQ, Preparation of reports and ensuring timely approval of the same. Compilation of records and Qualification Documents.
8. To organize and maintain the files of Qualification documents to initiate the project QMS documentation under the guidance of QA and Support for project QMS documentation.
9. Participation in execution of PQ, compilation of records and preparation of report, ensuring timely approval of report.
10. Participation in Engineering runs and Media fills, Compilation of various records and submitting to QA for preparation of reports.
11. Preparation of Project related QA documents in consultation with CQA, Site QA.
Also Read: Glenmark Pharmaceuticals – Hiring Pharmacovigilance Freshers & Experienced B.Pharm, M.Pharm, B.Sc, M.Sc Life Science Candidates
We are currently looking for a motivated and experienced individual to fill this important role in our organization (Manufacturing). We are conducting a walk-in interview on 02 April 2023, at Hotel Ginger, Baruch for the department of Production – Injectables (SVP), Oral Solid Dosage (OSD) & Effervescent Plants, Dahej.
If you are passionate about your work and are looking for an opportunity to grow in your career, then this is the right platform for you.
Position Details:
Injectables (SVP)
- Officer – 14 ( Experience 1 – 2 yrs)
- Sr. Officer/Executive – 3 ( Experience 3 – 7 yrs)
- Sr. Executive – 2 ( Experience 8 – 11 yrs)
- Manager/ Asst. Manager – 1 ( Experience 12 – 18 yrs)
Oral Solid Dosage (OSD)
- Reviewer – 3 ( Experience 2 – 4 yrs)
Effervescent
- Sr. Officer / Executive – 2 ( Experience 3 – 7 yrs)
Requirements:
- Minimum educational qualification: B.Pharm/M.Pharm.
- Prior experience is required.
- Knowledge of cGMP, safety regulations, and quality standards.
- Ability to work in a team and communicate effectively.
Job Description:
1. Handling and Participant in the calibration of instrument and Equipment.
2. Responsible for job allocation of production team.
3. To ensure the cGMP at all level in the injectable plant.
4. Active participant in the calibration of instrument, Validation of plant, vessel and machineries like Autoclave, Ampoule/Vial Washing Machine, Depyrogenation Tunnel, Ampoule/Vial Filling Machine, Mobile trolley.
5. Perform the IQ, OQ, PQ of machines i.e. Ampoule/vial Machine, Sterilization tunnel, Ampoule/Vial Filling machine, AHU, RABS, LAF, CIP & SIP, Weighing Balance.
6. Handling of media fill activity and area validation.
7. Responsible for Media fill & production related activity.
8. Preparation and periodic review of production SOP.
9. Responsible for GMP related online documentation like BMR and Log book.
10. Prepare protocol and active participant in Process validation, cleaning validation and equipment validation.
Also Read: 50 Openings @ UMEDICA Laboratories – Walk-In on 2nd April 2023 for Multiple Departments for B.Sc / M.Sc / B.Pharm / M.Pharm / ITI / Diploma / BE / ME Freshers & Experienced candidates
We are conducting a walk-in interview on 02 April 2023, at Hotel Ginger, Baruch for the position of Operators- Production SVP. We are seeking candidates who are skilled, experienced and possess excellent technical and interpersonal skills.
Position Details:
- Vial Filling Operator – 3
- Vial Sealing Operator – 3
- Vial Manufacturing Operator – 4
- Vial Washing Operator – 3
- Lyophilizer Operator – 3
- Autoclave Operator – 3
Requirements:
- Minimum educational qualification: ITI/Diploma.
- 2-5 years of working experience in SVP formulation.
- Prior experience in operating vial machines.
- Knowledge of cGMP, safety regulations, and quality standards.
- Ability to work in a team and communicate effectively.
Job Description:
1. Active Participant in the calibration of instrument and Equipment.
2. Validation of vessel and machineries like Autoclave, Ampoule/Vial Washing Machine, Depyrogenation Tunnel, Ampoule/Vial Filling Machine, Vial sealing Machine, Row to Row and area.
3. Participant in media fill and area validation.
4. Responsible for Media fill & production related activity.
5. Responsible for GMP related online documentation like BMR and Log book.
6. Operation and maintenance of Ampoule/Vial filling machine, Vial Sealing machine, Row by Row system.
7. Active participant in Process validation, cleaning validation and equipment validation.
8. Pre and Post cleaning and sanitation of Ampoule/Vial filling machine, vial sealing machine & Row by Row system.
9. After completion of autoclave cycle, unloading the load. (Like: Garment load, Machine parts load, Disinfectant load and Miscellaneous material load etc.)
10. Active Participant in calibration, qualification, validation and requalification activity at site.
11. Handling of filter integrity machine & perform the all type of filters integrity as per the SOP.
12. To perform area cleaning & sanitization as per the SOP.
13. Filtration of Disinfectant and IPA as per SOP and distribute the disinfectant and IPA.
14. Responsible for material & equipment movement in aseptic area as per the SOP.
15. Responsible for Aseptic
Please bring your updated resume and educational certificates to the venue. We offer competitive salaries and a dynamic work environment that fosters growth and learning.
Don’t miss this opportunity to join our team of skilled professionals. We look forward to meeting you at the interview.
More Job Updates Join What’s App Group – Click Here
Join Telegram Group – Click Here
