- Location
- Ankleshwar, India
- Type
- Full-time
- Department
- Manufacturing
- Source
- Workday
Description
JOB TITLE
Executive- Quality Control, Pharma
JOB PURPOSE
Generic
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.
REQUIREMENTS
Education / Experience
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 skills &
Competencies / Language
- Technical competence
- Leadership skills
- Analytical ability
- Planning ability
- Communication skills
- Problem solving
- Team Building
KEY ACCOUNTABILITIES
1.Analysis and approval
Sampling, analysis and ascertaining quality of raw materials, packaging material, intermediates, In-process samples and API for Chemistry Ankleshwar. Testing of the method validation samples and process validation samples and cleaning validation. Perform analysis and documentation of API finished product stability study as per stability study protocol. Coordinating with Production, Stores and QCAA for Approval / Rejection of raw materials/finished product. Validation and verification of analytical procedures as per requirement. Reporting OOS / OOT results and deviations. Maintaining retained samples as per standard procedure. Assisting in investigation of customer complaint. Testing of new samples (Vendor approval) Training of subordinates Give required suggestion for corrective actions and to plan effective preventive actions for the up gradation of the quality system. To ensure proper maintenance of the stability samples and their management. Disposal of waste according to the approved procedures. Continual reduction in the waste generation and effluent management. Co-ordination with microbiology lab (Pharmaceuticals) for microbial analysis of products and utilities. DocumentationGeneration, 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
Statutory documentation and management
QMS activities
Laboratory ManagementQualification 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
Quality, HSE and ComplianceAdhere 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
Team memberMember of validation team.
Participating in discussions and giving feedback to Manager, Quality control regarding on-going activities.
Other projectsSupporting 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