Base Career helps you apply smarter for this job.
Key skills for this role
To perform QC activities in order to ensure quality of products and services and maintain related documentation to adhere to quality operations and regulatory requirements.
All above activity shall be done living Group’s Values and Code of Ethics.
POST GRADUATE IN CHEMISTRY/PHARMACY
Experience: 3-5 years in a Quality Control/Analysis laboratory in a cGMP/ISO environment, with exposure to method development and validation activities
Technical competence
Leadership skills
Analytical ability
Planning ability
Communication skills
Problem solving
Team Building
Generation, managing and archiving Documents including raw data, reports, COA etc as per requirements.
Preparation and implementation of the SOPs in the laboratories system.
Specification preparation and implementing for API raw material and API finished product according to requirement.
Maintaining LIMS data entries
Providing technical support in compiling Annual Product Review.
Analytical method development when required.
Executing on line documentation
Skip the repetitive application forms
Install the Base Career Chrome Extension and autofill job applications across major job boards with your profile.
Trusted by over 500,000 job seekers on Base Career
More from this employer
Ankleshwar, IND
Ankleshwar, IND
The employer is seeking a pharmaceutical production professional to deliver production schedules, maintain quality and regulatory compliance, and improve yield. The role requires pharmaceutical manufacturing experience,
Ankleshwar, IND
Ankleshwar, IND
Ankleshwar, IND
Ankleshwar, IND
Ankleshwar, IND
Ankleshwar, IND
Ankleshwar, IND
Ankleshwar, IND
Statutory documentation and management
QMS activities
Qualification and Validation of instruments/equipment’s
Appropriate training and guidance to the subordinates.
Safety in the laboratory.
Regular housekeeping and upkeep of the work area.
Maintaining adequate inventory of chemicals and reference standards.
Adapting relevant technologies and systems in Quality control.
Laboratory equipment calibration and their maintenance.
Generate up gradation plans as need basis.
Any other activity assigned by the In charge, Quality control
Adhere to current GMP guidelines
Following ALCOA+++ practices during documentation and related activities
Compliance to local and international HSE norms
Regulatory compliance
ISO 14000 related activities
Regular Pharmacopoeia and regulatory requirement review for compliance
To participate in any regulatory/Customer inspection takes place at the site
Training of self and subordinates on quality and HSE systems
Member of validation team.
Participating in discussions and giving feedback to Manager, Quality control regarding on-going activities.
Supporting new projects (analytical method development (need base), validation, verification)
Laboratory compliance by reviewing documents for completeness
Preventive maintenance, Instrument calibration
New Instrument Qualification
Coordination with OEMs/Service providers for timely services
Private European pharmaceutical company developing, manufacturing, and supplying affordable generic, specialty, and over-the-counter medicines.
Visit company websiteJobs and hiring trendsFull-time
Mid · 3+ years experience
Onsite
Apply faster on company sites with our extension.