Executive - QC (Chemistry)

2.0 years

0.0 Lacs P.A.

Ankleshwar, Gujarat

Posted:4 days ago| Platform:

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Skills Required

Laboratory experienceMaster's degreeAnalysis skillsQuality controlAPIsLeadershipCommunication skills

Work Mode

On-site

Job Type

Full Time

Job Description

JOB DESCRIPTION JOB TITLE Executive-I, Quality Control, Chemistry Country India Site / Unit Chemistry Ankleshwar Job Family / Sub Job Family Quality Operations Standard job Quality Control JOB PURPOSE Generic To perform QC activities in order to ensure quality of products and services and maintain related documentation to adhere to QO and regulatory requirements. All above activity shall be done living Group’s Values and Code of Ethics. Specific additions (if needed) N/A KEY ACCOUNTABILITIES 1.Analysis and approval Supporting in-process control sample testing by online analysis to support production activities in all 3 shifts Sampling, analysis and ascertaining quality of water, 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, CWH and QA 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) 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. Documentation 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. 2.6.Executing on line documentation Laboratory Management Qualification and Validation of instruments/equipment 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. Developing training modules for improvement / training for HSE and Quality systems Generate up gradation plans as need basis. Any other activity assigned by the In charge, Quality control Quality, HSE and Compliance 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 Team member Member of validation team. Member of Analytical transfer team. Participating in discussions and giving feedback to Manager, Quality control regarding on-going activities. Other projects Trouble shooting activities. Participation in Industrial Excellence projects. Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations Plant round in absence of QA and during IInd and IIIrd shift. Online checking of critical process parameters during round. REQUIREMENTS Education / Experience M.Sc. Analytical/Organic Chemistry/Inorganic Chemistry Min. 2 years’ Experience in a Quality Control/Analysis laboratory in a cGMP/ISO environment Technical skills & Competencies / Language Technical competence Leadership skills Analytical ability Planning ability Communication skills Problem solving Team Building Behavioural Competencies (LEAD and others) Leveraging group values ‘Accountability, Authenticity, Collaboration, Courage and Trust’ during day to day operations

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