Analyst Ii, Qc Laboratory Services

1 week ago

Winnipeg, Canada Emergent Biosolutions Full time

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.
Job Summary
We are seeking a qualified individual to perform GMP-compliant testing to support raw material testing, in-process controls, finished product release, stability studies, and nonclinical/clinical studies, as well as assay and process validations. The role involves maintaining accurate laboratory documentation, performing preventive maintenance, and calibrating laboratory equipment according to established procedures. Additional responsibilities include contributing to and authoring investigations, deviations, critical reagent and standard qualifications, validation/verification protocols, supplier qualifications, CAPAs, and change controls.

**Responsibilities**:
Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.
- Receive test samples, standards, chemicals, and reagents; maintain accurate laboratory records and inventory for all laboratory materials.
- Demonstrate proficiency when performing analytical test methods with mínimal supervisory guidance.
- Be proficient in a variety of analytical/biological/Compendia methodologies and techniques.
- Report results and complete LIMS data entry in a timely manner. Perform peer review of QC data, review, and approval in LIMS.
- Adhere to all effective STM’s/SOPs and safety requirements and document laboratory work consistent with cGMP requirements.
- Perform preventative maintenance / calibration on laboratory equipment and demonstrate proficiency in their use and maintenance in accordance with established procedures.
- Execute critical reagent and standard qualification studies and write protocols/reports with supervisory or senior analyst guidance.
- Maintain a clean and sanitary work area in accordance with standard laboratory practice and procedures.
- Make detailed observations during performance of experimental tasks; obtain and interpret experimental data with supervisory guidance.
- Contribute to and provide input for troubleshooting/laboratory investigation efforts. Perform investigative testing as assigned.
- Write clear and concise assay forms, TMDs, and SOPs. Contribute to protocols, technical studies, and reports under supervisory or senior analyst guidance. Revise lab documentation including assay forms, test method documents, and standard operating procedures in accordance with document management procedures.
- Provide training and assistance to peers and junior staff in an effective manner.
- Execute development and validation studies and contribute to protocols/reports.
- Identify opportunities for improvements within QC procedures and documentation.
- Perform assigned tasks effectively with mínimal supervision.

The above statements are intended to describe the general nature of work performed by those in this job. It is not an exhaustive list of all duties, and other duties may be assigned.
Education, Experience & Skills
- University degree or technical diploma in chemistry, biology, microbiology, or related field of study.
- Minimum two to four years of directly related experience in a recognized professional or technical/scientific field. Experience in a pharmaceutical cGMP environment is an asset, but is not required.
- Proficient in Microsoft Office - Word, Excel, PowerPoint.
- Knowledge of pharmaceutical GMPs.
- Knowledge of regulatory guidance.
- Knowledge of laboratory techniques and safety precautions.
- WHMIS and biohazard safety awareness.
- 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.
- Able to multi-task and adapt to changing priorities.
- Able to communicate and articulate information in both written and verbal forms.
- Strong organizational and interpersonal skills; can work collaboratively with others.
- Able to interpret analytical data to support research and development work.
- Able to contribute ideas/solutions to aid in troubleshooting and investigations.

A Pre employment medical is required for this role.

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