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Analyst Ii, Qc Laboratory Services
Company | Emergent BioSolutions |
Address | Winnipeg, Manitoba, Canada |
Employment type | FULL_TIME |
Salary | |
Category | Biotechnology |
Expires | 2023-06-17 |
Posted at | 11 months ago |
Those who join Emergent BioSolutions feel a sense of ownership about their future. You will excel in an environment characterized by respect, innovation and growth opportunities. Here, you will join passionate professionals who advance their scientific, technical and professional skills to develop products designed-to protect life.
- Perform identification, assay and limit testing of raw materials and packaging components to support manufacturing requirements.
- Perform preventative and corrective maintenance on laboratory equipment.
- Execute development and validation studies and write protocols/reports; review and provide feedback.
- Maintain laboratory records and inventory for standards, reagents and laboratory supplies.
- Independently move projects forward.
- Work productively with other team members as well as on independent assignments; increased level of independence/productivity compared to Analyst I.
- Train and provide assistance to junior staff.
- Document laboratory work consistent with GxP requirements.
- Solve and clarify problems in collaboration with other departments.
- Well versed in a wide variety of analytical and compendial methodologies and techniques such as FTIR, pH measurement, refractometry, density/specific gravity measurement using density meter, UV-VIS, distillation, titrations, HPLC and GC.
- Write clear and concise SOPs; adhere to all effective SOPs and safety requirements.
- Execute tasks with a focus on departmental objectives.
- Make detailed observations, consistently analyzing and interpreting data.
- Guide project progression through appropriate decision making.
- Provide input on lab requirements and improvements.
- Maintain a clean and sanitary work area in accordance with standard laboratory practice and procedures.
- Communicate professionally, verbally and in writing, with collaborators and external departments.
- Maintain current understanding of regulatory requirements.
- Use experience and knowledge to investigate in order to identify the root cause of complex problems.
- Perform tasks effectively with minimal supervision.
- Able to interpret analytical data, reviewing a variety of identifiable factors.
- Able to provide training to peers in an effective manner.
- Comprehensive knowledge of pharmaceutical GLPs and GMPs.
- Able to communicate and articulate information in both written and verbal forms.
- University degree or technical diploma in chemistry, biology or related field of study.
- Knowledge of regulatory guidance.
- Proficient in complex procedures and problem solving.
- WHMIS and chemical safety awareness.
- Minimum of 2 - 4 years directly related experience in a recognized professional or technical/scientific field.
- Strong organizational and interpersonal skills and the ability to work collaboratively with others.
- Comprehensive knowledge of laboratory techniques and safety precautions.
- Competent in laboratory safety and generally-accepted lab practice, including maintaining adequate written laboratory records.
- Ability to work in a fast-paced and highly regulated environment.
- Experience in a pharmaceutical cGMP environment is an asset.
- Able to multi-task and adapt to changing priorities.
- Strong leadership skills, independence and initiative.
- Proficient in Microsoft Office - Word, Excel, PowerPoint.
- Medical assessment req’d upon hire.
- Citizenship/Permanent Resident or Valid Work Permit.
- Successful Completion of a Criminal Record Check.
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