Supervisor, Formulations

121 Altasciences Preclinical Scranton, Inc

Scranton (Lackawanna County)

On-site

USD 90,000 - 120,000

Full time

4 days ago
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Benefits offered by this job

Health/Dental/Vision Insurance Plans
401(k)/RRSP with Employer Match
Paid Vacation and Holidays
Paid Sick and Bereavement Leave
Employee Assistance & Telehealth
Telework when applicable.

Job summary

121 Altasciences Preclinical Scranton, Inc seeks a hands-on Supervisor, Formulations to lead dose formulation and test material management for preclinical studies in a CRO setting.

You will mentor staff, help establish a new laboratory, and drive SOP development to ensure GLP compliance and high-quality results across teams.

Qualifications

  • Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or related field.
  • 2-3 years hands-on formulations experience.
  • Experience in a CRO environment preferred.
  • Experience preparing dose formulations and managing test articles.
  • Experience training, mentoring, or leading laboratory personnel.
  • Experience developing, reviewing, and updating SOPs.
  • Familiarity with GLP regulations and regulated lab environments.
  • Strong organizational and time-management skills with multiple priorities.
  • Excellent communication and collaboration across teams.
  • Proficiency with Microsoft Office applications (Word, Excel, Outlook, PowerPoint).

Responsibilities

  • Supervise daily dose formulation and test material management activities in support of preclinical studies.
  • Prepare and oversee preparation of test article formulations, vehicle formulations, and chemical solutions per study protocols.
  • Assist with setup and expansion of a new laboratory, including workflows, equipment organization, and lab best practices.
  • Develop, review, update, and maintain SOPs to support operations and regulatory compliance.
  • Train, mentor, and provide day-to-day guidance to Formulations staff.
  • Manage receipt, inventory, storage, retention, and disposition of test materials.
  • Support DFA activities and ensure accurate documentation and sample tracking.
  • Collaborate with Study Directors and cross-functional teams to meet study timelines and client expectations.
  • Monitor laboratory supplies, equipment maintenance, and readiness.
  • Identify opportunities for process improvements and efficiencies.

Skills

Formulations
Leadership
GLP compliance
Mentoring
Documentation

Education

Bachelor's degree in Chemistry/ Biology/ Pharmaceutical Sciences

Tools

Microsoft Office

Job description

About The Role

We are seeking a hands‑on and pragmatic Supervisor, Formulations to support dose formulation, test material management, and laboratory operations within a fast‑paced Contract Research Organization (CRO) environment.

This role is ideal for an experienced laboratory professional with prior formulations experience who is looking to expand their leadership responsibilities while remaining actively involved in laboratory operations.

As a key member of the team, you will oversee daily formulation activities, support preclinical studies, mentor laboratory staff, and contribute to the successful setup and growth of a new laboratory.

You will also play an important role in developing, updating, and maintaining Standard Operating Procedures (SOPs) to support operational excellence and regulatory compliance.

What You'll Do
  • Supervise daily dose formulation and test material management activities in support of preclinical research studies.
  • Prepare and oversee the preparation of test article formulations, vehicle formulations, and chemical solutions according to study protocols.
  • Assist with the setup and expansion of a new laboratory, including implementation of workflows, equipment organization, and laboratory best practices.
  • Develop, review, update, and maintain SOPs to support laboratory operations and ensure compliance with regulatory requirements.
  • Train, mentor, and provide day‑to‑day guidance to Formulations Research Associates and laboratory personnel.
  • Manage the receipt, inventory, storage, retention, and disposition of test materials.
  • Support Dose Formulation Analysis (DFA) activities and ensure accurate documentation and sample tracking.
  • Collaborate with Study Directors and cross‑functional teams to meet study timelines and client expectations.
  • Monitor laboratory supplies, equipment maintenance, and operational readiness.
  • Ensure all activities are performed in accordance with GLP regulations, company policies, and quality standards.
  • Identify opportunities for process improvements and operational efficiencies within the laboratory.
What You'll Need to Succeed
  • Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or a related scientific discipline.
  • 2-3 years of hands‑on formulations experience is required.
  • Experience working within a Contract Research Organization (CRO) environment is strongly preferred.
  • Demonstrated experience preparing dose formulations and managing test articles in support of regulated studies.
  • Experience training, mentoring, or leading laboratory personnel.
  • Experience developing, reviewing, and updating SOPs and laboratory documentation.
  • Familiarity with laboratory start‑up activities, process implementation, and workflow improvements is preferred.
  • Working knowledge of GLP regulations and regulated laboratory environments.
  • Strong organizational and time‑management skills with the ability to manage multiple priorities in a fast‑paced setting.
  • A pragmatic, solution‑oriented approach to problem‑solving and decision‑making.
  • Excellent communication and interpersonal skills with the ability to collaborate effectively across teams.
  • Proficiency with Microsoft Office applications, including Word, Excel, Outlook, and PowerPoint.
  • Detail‑oriented, adaptable, and committed to delivering high‑quality scientific results.
Work Authorization & Sponsorship

Applicants must be legally authorized to work in the United States. Altasciences is unable to provide sponsorship, sponsorship transfers, or visa maintenance for this position. All applicants must possess valid work authorization that does not require employer sponsorship now or in the future.

Benefits

Benefits Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Benefits Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

  • Health/Dental/Vision Insurance Plans
  • 401(k)/RRSP with Employer Match
  • Paid Vacation and Holidays
  • Paid Sick and Bereavement Leave
  • Employee Assistance & Telehealth Programs
  • Telework when applicable.
Incentive Programs

Altasciences' Incentive Programs Include: Training & Development Programs Employee Referral Bonus Program #LI-JR1

At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well‑being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences.

Altasciences is an equal opportunity employer committed to diversity and inclusion.

Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives.

All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation.

Reasonable accommodations for persons with disabilities during the recruitment process are available upon request.

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