• Investigate quality issues within manufacturing and quality laboratories

• Examine deviations, out-of-specification results, and atypical investigations

• Identify root causes and suggest effective corrective action plans

• Ensure all reports comply with regulatory requirements and company policies

• Contribute to moderately complex projects, managing your own time to meet targets

• Develop plans for short-term work activities within a collaborative team environment

• Apply skills and discipline knowledge to contribute to work within the Work Team

• Make decisions to resolve moderately complex problems in standard situations

• Work under general supervision, following established procedures and general instructions.

Here Is What You Need (Minimum Requirements)

• B pharm/ M pharm/ M.Sc. with at least 6 years of experience.

• Proven record of problem-solving and decision-making skills

• Experience in the pharmaceutical industry

• Strong background and knowledge in manufacturing, compliance, and technology investigations, processes, and systems

• Ability to work both independently and collaboratively

• Effective communication skills, both written and verbal

• Computer literate with superior skills in managing Excel spreadsheets

Bonus Points If You Have (Preferred Requirements)

• Experience with investigations, including conducting and writing investigations using methodology

• Familiarity with regulatory requirements and quality standards

• Strong analytical and critical thinking skills

• Ability to manage multiple projects simultaneously

• Experience with root cause analysis and corrective action plans

• Excellent organizational skills

• Ability to mentor and guide junior colleagues

• Strong interpersonal skills and the ability to foster a collaborative team environment