Chemist

Job Title: Chemist I – Quality Control Laboratory Job Description early-career chemist to gain hands-on experience in a GMP-regulated pharmaceutical environment, with significant exposure to HPLC, stability programs, validation activities, and industry-standard laboratory systems in a collaborative, fast-paced setting. Responsibilities Perform routine analytical testing of raw materials, in-process samples, bulk products, finished products, and stability samples in a GMP-regulated pharmaceutical laboratory. Execute testing using established analytical methods and laboratory instrumentation, including HPLC and other analytical techniques as required. Accurately document test results and maintain complete, legible, and compliant laboratory records in accordance with GMP and data integrity requirements. Support investigations related to out-of-specification (OOS) or atypical results by providing accurate data, participating in root-cause analysis, and assisting with corrective actions. Assist with validation activities, including method validation, method transfers, and other special projects to support new or existing products and processes. Maintain laboratory equipment in good working order, including routine cleaning, basic troubleshooting, and coordination of calibration and preventative maintenance activities. Review analytical data for accuracy, completeness, and compliance with established specifications and procedures prior to submission or approval. Adhere at all times to GMP, SOPs, quality standards, safety procedures, and regulatory requirements while performing laboratory activities. Collaborate closely with QC colleagues, QA, and manufacturing personnel to ensure timely completion of testing to support production and stability programs. Effectively manage multiple testing assignments and priorities in a fast-paced laboratory environment while meeting timelines and quality expectations. Contribute to a culture of continuous improvement by identifying opportunities to enhance laboratory processes, documentation practices, and data integrity. Essential Skills Diploma or Degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline. Previous laboratory experience gained through industry, co-op, internship, or academic research. Hands-on experience performing analytical testing in a GMP-regulated pharmaceutical laboratory or strong familiarity with GMP principles and laboratory best practices. Exposure to HPLC and other analytical instrumentation, with the ability to follow established analytical methods. Strong attention to detail with excellent documentation practices and a clear understanding of data integrity requirements. Ability to manage multiple priorities and testing assignments in a fast-paced laboratory setting. Strong analytical and problem-solving abilities to support investigations and resolve technical issues. Proficiency with Microsoft Excel and Microsoft Office for data handling, reporting, and documentation. Ability to work effectively in a collaborative, team-oriented environment and to communicate clearly with QC, QA, and manufacturing personnel. Additional Skills & Qualifications Experience performing analytical testing specifically in a GMP-regulated pharmaceutical QC laboratory. Practical, hands-on HPLC experience, including sample preparation, instrument operation, and basic troubleshooting. Experience or familiarity with Empower chromatography data software. Experience or familiarity with LIMS (Laboratory Information Management Systems) for sample and data management. Experience supporting validation activities, method transfers, and special laboratory projects. Experience supporting investigations into OOS or atypical results within a quality-controlled environment. Strong organizational skills and the ability to balance a high volume of testing while maintaining quality and compliance. Interest in developing a career in pharmaceutical quality control, stability testing, and GMP-regulated environments. Work Environment This position is 100% on-site and requires daily presence in the Quality Control laboratory to support testing activities and close collaboration with the QC team. The role follows a day shift schedule aligned with standard business hours, approximately 8:00 AM to 4:30 PM, Monday through Friday, with some flexibility as needed. Work takes place in a GMP-regulated pharmaceutical manufacturing setting where strict adherence to GMP, SOPs, safety procedures, and documentation requirements is essential. The laboratory environment is fast-paced and manages a high volume of testing to support manufacturing operations and stability programs, requiring strong organization and the ability to handle multiple priorities. The culture is highly collaborative, with the Chemist I working closely with experienced chemists, supervisors, QA, and manufacturing personnel, and receiving guidance, training, and support to develop technical and professional skills.\ Job Type & Location This is a Contract position based out of Cambridge, ON. Pay And Benefits The pay range for this position is $23.00 - $30.00/hr. Workplace Type This is a fully onsite position in Cambridge,ON. À propos d'Actalent Actalent est un leader mondial dans les services d’ingénierie et de sciences ainsi que dans les solutions de talents. Nous aidons des entreprises visionnaires à faire progresser leurs initiatives d’ingénierie et de science grâce à l’accès à des experts spécialisés qui favorisent l’échelle, l’innovation et la rapidité de mise sur le marché. Avec un réseau de près de 20 000 consultants et 5 000 clients à travers les États-Unis, le Canada, l’Asie et l’Europe, Actalent dessert de nombreuses entreprises du Fortune 500. Nous sommes fiers d’être l’une des 500 meilleures firmes de conception de l’Engineering News-Record (ENR) pour nos services de conception en ingénierie et un lauréat du prix ClearlyRated Best of Staffing® tant pour le service client que pour les talents. Actalent est un employeur souscrivant au principe de l’égalité des chances et accepte toutes les candidatures sans tenir compte de la race, du sexe, de l’âge, de la couleur, de la religion, des origines nationales, du statut d’ancien combattant, d’un handicap, de l’orientation sexuelle, de l’identité sexuelle, des renseignements génétiques ou de toute autre caractéristique protégée par la loi. Si vous souhaitez faire une demande d’accommodement raisonnable, tel que la modification ou l’ajustement du processus de demande d’emploi ou d’entrevue à cause d’un handicap, veuillez envoyer un courriel à [email protected] pour connaître d’autres options d’accommodement. Ordonnance sur l’égalité des chances de San Francisco: Conformément à l’Ordonnance sur l’égalité des chances de San Francisco, pour tous les postes situés dans la ville et le comté de San Francisco, nous examinerons les candidatures des personnes qualifiées ayant un casier judiciaire ou des antécédents criminels. Utilisation de l’intelligence artificielle (IA): Nous pouvons utiliser l’intelligence artificielle (IA) pour soutenir certaines étapes de notre processus d’embauche, notamment la recherche, la présélection et l’évaluation des candidatures. L’IA aide à analyser les candidatures et les qualifications, mais les décisions finales sont prises par notre équipe de recrutement. En soumettant votre candidature, vous reconnaissez et acceptez que celle-ci puisse être examinée à l’aide d’outils d’IA. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Perform routine analytical testing of raw materials, in-process samples, and finished products within a GMP-regulated pharmaceutical laboratory. Support validation activities and investigations into out-of-specification results while maintaining compliant laboratory records.

Requires a diploma or degree in Chemistry, Biochemistry, or Pharmaceutical Sciences with previous laboratory experience. Candidates should have hands-on experience with HPLC and a strong understanding of GMP principles and data integrity.

• Microsoft ExcelSouhaitée

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• HPLC
• GMP
• Analytical Testing
• Data Integrity
• Method Validation
• OOS Investigations
• Empower Software
• LIMS
• Sample Preparation
• Microsoft Excel
• Quality Control
• Pharmaceutical Analysis

• Science & Research
• Manufacturing
• Engineering
• Healthcare
• Consulting

Formation minimale

Baccalauréat

Expérience minimale

0+ ans

Postuler avant le

12 sept. 2026

Langue de l’offre

anglais

Heures de travail

40 heures par semaine

Niveau d’expérience

Entry level