3 Opening(s)
3.0 Year(s) To 6.0 Year(s)
2.40 LPA TO 3.00 LPA
Hiring for Quality Executive in Glucose & Starch Powder Manufacturing Industry
Position: Quality Executive 02
Education – BSC Chemistry
Experience: Min 3 Years in Quality Assurance, Documentation & Audit
Skill: COPA, Audit, etc
Job responsibility:
Handling of Change Control.
Data compilation of annual product review report.
Batch Release
Co-ordination and participation in validation activities.
Logbook issuance and retrieval.
Participation in line ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: Production Officer (Documentation)
Location: Vapi
Experience: 5 - 8 Years
Industries: Pharma - API
Responsibilities.
Handling of QAMS, DMS activities
Prepare SOP, BMR, ECR and all related docs. as per CGMP
TO maintain & review all document like change control, Incident with compliance report
Involvement in ...
1 Opening(s)
20.0 Year(s) To 25.0 Year(s)
18.00 LPA TO 22.00 LPA
Good Knowledge of USFDA/ EDQM /ANVISA / and all other regulatory & CGMP awareness.
Strategic oversight and leadership: Develop and implement the company's quality management system (QMS) and strategy, aligning it with business objectives. This includes overseeing all aspects of quality operations and managing the QA and QC departments.
Regulatory compliance: Ensure ...
1 Opening(s)
15.0 Year(s) To 25.0 Year(s)
15.00 LPA TO 20.00 LPA
To review and implement a Quality Management System for cGMP compliance at the Production (Injectable) plant.
To prepare, Review and Approve BMR, BPR and related documents.
Handling of Caliber QAMS, DMS, Nichelon 5 CMS, Dynamic, Schedule and Track and trace Serialization & aggregation.
Giving the required training also Responsible for Media fill and ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Responsibilities: • Ensure effective implementation of QMS elements such as deviation, CAPA, change control, and risk assessment in production. • Support production teams in initiating and closing QMS records in a timely manner. • Coordinate with QA and cross-functional teams to ensure proper documentation and follow-up of QMS activities. • ...
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 ...
4 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 6.00 LPA
M. Sc. / B. Pharm / M. Pharm: 4 - S yrs. of Exp. in QA Documentation, SOP preparation, Change Control, and CAPA, possess knowledge of production prcuzess, experience on activiEes (Analytical'O, handling ISO audits.Doc
M. Sc. / B. Pharm / M. Pharm: 4 - S yrs. of Exp. in QA ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
1.80 LPA TO 2.40 LPA
JOB DESCRIPTION
HPS/2024/87
Quality Cheker
Male
1
1 to 3
DME
Masat
Job Role :-
Industry Type - Enameled Round Winding Wires
Enameled Round Copper Wires are used in electrical machines such as motors, generators, transformers, household appliances, auto-electrical, refrigeration (hermetic) motors, electrical hand tools, fans, switch gears, coils & relays, ballasts, and more, mainly in low voltage applications.
Enameled Rectangular ...
1 Opening(s)
6.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 7.00 LPA
Position: Microbiologist Incharge (U1)
Location: Daman
Experience: 6 - 8 Years
Industries: Pharma
Responsibilities:
Verified testing activity performed by Microbiology team:
a. Environmental Monitoring
b. Water Analysis (Microbiology)
c. Sub culturing
d. Personnel Monitoring
e. Growth Promotional Test
f. Bioburden Test.
g. Moisture Analysis of rubber Stopper.
h. Liquid Particle count of rubber stopper.
i. Sterility test of ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
5.00 LPA TO 5.40 LPA
Position: Executive - Microbiologist
Location: Pandhurna
Experience: 3 - 4 Years
Industries: Pharma Packaging
Responsibilities:
Verified testing activity performed by Microbiology team:
a. Environmental Monitoring
b. Water Analysis (Microbiology)
c. Sub culturing
d. Personnel Monitoring
e. Growth Promotional Test
f. Bioburden Test.
g. Moisture Analysis of rubber Stopper.
h. Liquid Particle count of rubber stopper.
i. Sterility ...