TERM - Analyst I, QC Laboratory Services

Job summary

The Analyst I performs GMP-compliant laboratory testing to support raw material, in-process, and finished product release. They are also responsible for maintaining laboratory records, equipment, and inventory while adhering to safety and regulatory guidelines.

Job details

Preparedness today, safer tomorrow. Emergent is a leading public health company that delivers protective and life-saving solutions tocommunities around the world. Here, you will join passionate professionals where our culture is informed by our values and commitment to protecting and saving lives.Job Summary The Analyst I, QC Laboratory Services performs GMP compliant testing as required to support Raw Material testing, In-process, Finished Product release & Stability or nonclinical/ clinical studies. The Analyst I also perform testing required to support assay and process validations. He/She will perform testing to support release of lab specific material (media, standards). Responsibilities • Perform routine laboratory testing procedures including analyzing and reviewing data• Receive and test samples within required timeframes• Receive, prepare, test, release materials used for QC testing (for example: media, standards, biological indicators, cultures, etc.)• Document laboratory work consistent with GDP and GxP requirements• Maintain laboratory records, ensuring documents are reconciled and filed immediately after completion.• Maintain inventory of supplies, reagents, standards, solutions, cultures, etc required to perform testing• Perform preventative maintenance on laboratory equipment• Maintain a clean and sanitary work area in accordance with standard laboratory practice and procedures• Contribute to investigations to aid in determination of root cause• Adhere to all effective TMDs/SOPs and safety requirements• Maintain the lab and testing following applicable regulations and guidelines, including but not limited to USP, EP, GMP, FDA, Health Canada and EU requirements• Work effectively and productively with other team members and on independent assignments• Prepare and Autoclave supplies and garbage• Ability to successfully complete a pre-employment medical 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 microbiology, biology or related field of study• Experience in a pharmaceutical cGMP environment is an asset, but is not required.• Basic knowledge of Microsoft Office - Word, Excel• Basic knowledge of pharmaceutical GLPs and GMPs• Knowledge of laboratory techniques and safety precautions• WHMIS and biohazard safety awareness• Ability to work in a fast paced and highly regulated environment• Able to multi-task and adapt to changing priorities• Competent in laboratory safety and generally-accepted lab practice, including maintaining adequate written laboratory records• 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 dataThere are physical/mental demands and work environment characteristics that must be met by an individual to successfully perform the essential functions of the job. This information is available upon request from the candidate. As part of our team, you'll join talented and inspiring colleagues whose sense of purpose complements your own. We offer highly diverse career opportunities, a supportive culture, competitive salaries, flexible work arrangements and an extensive benefits package. Information submitted will be used by Emergent BioSolutions for activities related to your prospective employment. Emergent BioSolutions respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy.

What you’ll do

The Analyst I performs GMP-compliant laboratory testing to support raw material, in-process, and finished product release. They are also responsible for maintaining laboratory records, equipment, and inventory while adhering to safety and regulatory guidelines.

Requirements

Candidates must hold a university degree or technical diploma in microbiology, biology, or a related field. While pharmaceutical cGMP experience is an asset, it is not required, provided the applicant has basic knowledge of laboratory techniques and safety.

Benefits

• Competitive salaries
• Flexible work arrangements
• Extensive benefits package

Listed skills

• Data analysis · Preferred
• Communication · Preferred
• Multi-Tasking · Preferred
• Microsoft Office · Preferred
• Inventory management · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Microbiology
• Laboratory testing
• GMP compliance
• Data analysis
• Sample preparation
• Laboratory safety
• Inventory management
• Preventative maintenance
• SOP adherence
• Microsoft Office
• GLP
• Biohazard safety
• Multi-tasking
• Communication
• Organizational skills
• Analytical data interpretation
• Good Laboratory Practice (GLP)
• Laboratory Safety
• Process Validation
• Laboratory Equipment
• Microsoft Word
• Microsoft Excel
• Autoclaves
• Biological Hazards
• Biology
• Good Manufacturing Practices
• Clinical Trials
• Interpersonal Communications
• Inventory Management
• Laboratory Techniques
• Laboratory Testing
• Multitasking
• Pharmaceuticals
• Investigation

Job areas

• Science & Research
• Healthcare
• Manufacturing
• Quality Control Laboratory Analyst
• Quality Control Analyst
• Physical and Engineering Science Technicians Not Elsewhere Classified
• Quality Control Analysts
• Life, Physical, and Social Science Technicians, All Other

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