No Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.
We strongly uphold our core values of Empathy, Integrity, and Transparency, and we strive to create a collaborative, innovative, and inclusive work environment that fosters personal growth and development.
No deviation is seeking a dedicated and detail-oriented QC IPC Chemist for a 1 year Night shift only (8pm-8am) contract role in a leading pharmaceutical company. The ideal candidate will play a key role in ensuring the quality and compliance of products by supporting chemical analysis and testing according to regulatory standards. This is an excellent opportunity for a junior-level professional looking to gain valuable experience in the pharmaceutical industry.
By joining our team, you will have the opportunity to make a meaningful impact in the pharmaceutical industry while advancing your career.
Key Responsibilities:
- The IPC Chemist is responsible for ensuring that the manufacturing process remains consistent and meets predefined quality standards throughout the various stages of production. They perform tests and checks on samples taken during production to ensure that the intermediate stages align with quality specifications before the final product is manufactured.
- Conducts analytical testing using methods like HPLC, GC, FTIR, UV-Vis spectrometry, titrations, and other chemical assays to analyze the potency, purity, and identity of drug substances.
- Performs stability studies to assess how the quality of a drug substance or product changes over time under various environmental conditions.
- Tests for impurities, residual solvents, and microbial content to ensure compliance with regulatory guidelines.
- Prepares and maintains lab documentation, such as test results, standard operating procedures (SOPs), and analytical reports.
- Works in a controlled laboratory environment, following Good Laboratory Practices (GLP) and regulatory standards such as those from the FDA or EMA.
Qualifications and Experience:
- Diploma in Chemistry, Pharmaceutical Science, or a related field.
- Basic knowledge of analytical techniques such as HPLC, GC, UV, and wet chemistry.
- Familiarity with GMP, GLP, and relevant regulatory guidelines.
- Strong attention to detail, problem-solving skills, and ability to work independently.
- Excellent organizational skills and ability to maintain accurate documentation.
- Effective communication skills and a team-oriented mindset.
- Preferred Experience:
- Prior experience in a pharmaceutical or chemical laboratory setting is advantageous, but fresh graduates are welcome to apply.
- Contract Duration: 1 year, with potential for extension based on performance and business needs.
