1 Opening(s)
8.0 Year(s) To 12.0 Year(s)
7.00 LPA TO 8.50 LPA
Position: Sr. Executive/ Asst. Manager - QA
Location: Vapi
Experience: 8 - 12 years
Industries: Pharma API
Responsibilities:
QMS handling like, change control, deviation, market compliant, returned product, SMF, Quality manual, VMP, and New BMR , BPR preparations or revisions.
Audit work ,preparation for compliance ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: Executive/Sr. Executive - QA
Location: Vapi
Experience: 2 - 4 Years
Industries: Pharma - Formulation
Responsibilities:
Responsible for document and data control activities
To prepare and update all master document list as per requirement.
To initiate change control/document amendment for any change or improvement in the ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: QA Officer
Location: Sarigam near by Vapi
Experience: 3 -5 Years
Industries: Pharma
Responsibilities:
To perform IPQA activities at shop floor in each and every stage of manufacturing and packing.
QA overview for clean room behavior and personnel hygiene .
Review of batch processing records.
Review of all ...
1 Opening(s)
8.0 Year(s) To 12.0 Year(s)
12.00 LPA TO 14.00 LPA
Vacancy For DGM Production
Experaince in API Production is mandotory
B Pharma/M Pharma/Ph D Pharma is mandotory to apply.
Job location - Ambernath, Dist - Thane, Maharashtra
Age should be less than 40 year
Job Description
To organize, supervise and control the production activity till raw material dispensing to packing.
Monitor constantly the progress of monthly production plan and collaborate with subordinate in dealing with all shop floor problems.
Ensure that the products are manufactured and storage according to appropriate documentation.
Responsible for qualification and validation document review.
Daily monitoring of OAE and reporting to Production head.
Drive the production team to deliver operational excellence with quality and customer service targets.
Preparation of Quality Risk Assessment (QRA), APQR and support to perform Cleaning Validation, Process Validation activity.
Ensure the operations shall perform with documentation integrity.
Handling of Change Control, Audit compliances, Investigation of Deviation, OOS, Market Complaints etc.
Ensure departmental training for effectiveness of CAPA, SOP, HSE.
Provide opportunities for development of product team with particular emphasis on the process.
Develop team to solve day-to-day operational issues and planning of goals, organize and facilitate work team meetings.