Associate CQ Recruitment 2023

Job Responsibilities:

Manage the receipt, storage, and handling of raw materials, packing materials, in-process, finished, and stability samples.
Ensure training records are updated and correctly filed to reflect current testing capabilities.
Perform sampling and labeling of materials according to defined procedures and verify equipment and instruments.
Interpret and evaluate data for accuracy, precision, trends, and potential impacts on Good Manufacturing Practices (GMP) and recommend corrective actions.
Ensure all documentation and quality records are conducted in accordance with GMP and Good Laboratory Practices (GLP) requirements and filed as per existing policies.
Review and revise Standard Operating Procedures (SOPs), analytical methods, and related procedures/documents to keep them current.
Perform analyses on finished products, raw materials, and components, including data entry, review, and/or approval in a computerized database and generate EMS reports.
Contribute to the completion of complex projects, manage own time to meet agreed targets, and develop plans for work activities within a team.

Eligibility Criteria:

Bachelor’s Degree in Pharmacy and Master’s in Pharmacy or Master’s in Chemistry.
0 to 5 years of experience.

Preferred Skills:

Demonstrated technical skills in packing, raw material, in-process, stability, and finished product testing.
Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations.
Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.
Excellent organizational skills and strong ability to multitask.
Strong written and verbal communication skills.
Laboratory work experience with analytical HPLC (High-Pressure Liquid Chromatography) technique.
Experience leading continuous improvement projects.
Knowledge of lean manufacturing, Six Sigma methodologies, and statistics.