Stanford Laboratories Pvt. Ltd. is a WHO-GMP Certified company engaged into manufacturing & marketing of Pharmaceutical Formulations since more than 2 decades. Having a rich expertise in manufacturing of different profiles of Tablets , such as Sustained Release , Delayed / Extended Release, Enteric Coated, Film Coated etc. along with formulations of Capsules, Dry Syp. , Liquid Orals.
Executive: Production @ Stanford Laboratories Pvt. Ltd
- Experience: 2 to 7 yrs
- Openings: 05
Job description:
– Responsible for manufacturing and monitoring of batches in Tablet, Capsules, Liquid Oral, Ointment departments.
– Must have sound knowledge and experience in formulations.
– Must have experience in granulation and compression.
– To maintain the GMP, personnel safety and hygienic practices on shop floor.
– To ensure the online completion of documents.
– To provide the periodic training based on SOPs to the production personnel and maintain the record of same.
– To ensure that all breakdowns are immediately reported to QA/ maintenance and tracked till resolved.
– To ensure that preventive maintenance schedule and calibration schedule is implemented and equipments are offered to maintenance accordingly.
– To co-ordinate with QA, QC, Engg. and store department for smooth running of production activity.
Interested candidates, please mail your updated CV to hr@stanlabs.com
Executive QC @ Mehatpur, UNA(HP)
- Experience: 1 to 3 yrs
- Openings: 02
Job description:
– Should be having sound knowledge & experience on HPLC, GC, Chemical testing
– Review and Preparation of calibration report of HPLC, GC and other equipment.
– Having knowledge of trouble shooting on HPLC &GC.
– Knowledge of all equipment and instruments
Executive / Sr. Executive – IPQA for Mehatpur, H.P.
Job description:
Roles & Responsibilities:
-Preparation, Review and Issuing control of BMR and BPR
-Handling of Change control, Deviation, CAPA, and Investigation in shop floor.
-Preparation and Review of SOP and All formets of manufacturing and packing.
-Preparation and control of Validation protocol and involving in process validation.
-In process monitoring during Dispensing, Granulation, Compression, Coating and Hard gelatin capsule filling.
-Inprocess monitoring during packing operation.
Step wise line clearance in:
- Dispensing area
- Manufacturing area (Granulation, Compression, Coating, Inspection and Capsule filling area)
- Packing Area (Primary and secondary packing area)
-Swab and Rinse sampling.
-Inspection of packing goods for evaluation of physical attribution before and after completion of final packing.
-Finished product sampling and Batch record review.
-Sampling activity during in process and validation.
-Calibration of instruments (D.T, Friability, Hardness Tester and Weighing balance) as per schedule.
-To carry out validation batches sampling as per process validation protocol.
-To ensure in-process controls are performed during manufacturing operations and results are satisfactory.
-Overall responsibility to review BMR, Logbooks, In-process formats and other online records.
-To perform cleaning validation sampling as per cleaning validation protocol.
Required Candidate Profile:
Experience: Min 2 to 5 Years
Qualification: B. Pharma/ M. Pharma
Preferably Male Candidates
Executive / Sr. Executive: QA – QMS @ HP
- Experience: 2 to 5 yrs
- Openings: 02
Job description:
- Documentation, QMS Documentation, Validation, qualification, deviation, change control etc
2. MFR/SOP/AMV (analytical Method Validation), ACTD/CTD, Dossier Preparation.
3. Knowledge of COPP.
4. Having a sound knowledge of BMR preparation and filing, FR&D Documentation, PV ETC Monitoring of process validation activity with preparation of protocol and report.
5. Monitoring of cleaning validation activity with preparation of protocol and report.
6. Review the Qualification document of equipment and facility.
7. Review of instrument and equipment calibration.
8. Review and monitoring of Revalidation of process and requalification of equipment/instrument.
Industry Preferred: Pharma company only in pharma formulation of oral and solid.
Executive Warehouse @ Mehatpur, HP
- Experience: 2 to 5 yrs
- Openings: 02
Job description:
– Arrangement of dispatch of Finished Goods as per SOP, as well as preparing and responsible of finished goods.
– Dispatch Related activities
– handling of recalled material.
– Make an invoice in SAP and all documents in dispatch process.
– to establish and implement systems, SOP’s and documentation as per GMP.
– Any Graduate
– Knowledge of SAP is must
Machine Operators (Granulation/Compression/Coating) @ Mehatpur, UNA
- Experience: 2 to 7 yrs
- Openings: 10
Job description:
Roles and Responsibilities:
– Should know cGMP practices and Documentation.
– Handled USFDA Audits
– Should be able to enter data in BMR BPR independently
– Should be able to manage area independently
– Ready to work in shifts
Machines: Granulation
Vibratory sifter
RMG – Tapasya
FBP – Pam Glatt(ACG)
Blender- Tapasya,
Compression:
Cadmach
All with Auto weight control system
Capsule Filling:
AF 90T – ACG
Coating:
ACG- 48 inch, 60 inch
Packing
BQS – ACS
Strip – Satellite
Cartonator- High Carty & Vector- ACG
Desired Candidate Profile:
Qualification: ITI /+ 2 with 2 to 6 years of experience in Tablet Manufacturing at OSD Plant
Ready to work in Shifts
Freshers B.Pharm/ M. Pharma – Production @Mehatpur, Una
Job description:
- Excellent written and verbal skills
- Impeccable attention to detail and accuracy.
- Strong internet research skills
- Good Organizational, time management and priority setting skills, and the flexibility to multi – task in a fast -paced environment.
- Ability to think critically, work independently and follow instructions.
- Working knowledge of Microsoft Excel and Word.
- Familiarity with drug development process and associated pharmaceutical market.
Interested candidates can share their updated resume on hr@stanlabs.com, along with the below mentioned details
Total Work Experience:
Current Location:
Current CTC:
Expected CTC:
Notice Period:
Open to relocation to Una, Mehatpur (HP) :
