Supervisor, Formulations

Altasciences; Scranton, Northern (Lackawanna County, KY); Hybrid; USD 90,000 - 125,000; Full time

Benefits offered by this job

Health Insurance

Employer 401k with Employer Match

Paid Vacation and Holidays

Paid Sick Leave

Telehealth Programs

Telework when applicable

Job summary

Altasciences in Scranton, PA is seeking a hands-on Supervisor, Formulations to oversee dose formulation, test material management, and lab operations in a fast-paced CRO.

You will lead and mentor Formulations staff, help establish new lab workflows, write SOPs, ensure GLP compliance, and collaborate with Study Directors to meet client timelines.

Qualifications

• Hands-on formulations experience required.
• Experience in a CRO/GLP-regulated environment preferred.
• Ability to develop, review and maintain SOPs and supporting documentation.
• Strong mentoring and leadership capabilities.

Responsibilities

• Supervise daily dose formulation and test material management activities.
• Prepare and oversee formulation preparations according to study protocols.
• Assist with lab start-up, workflow implementations, and equipment organization.
• Develop, review and maintain SOPs for compliance and operational excellence.
• Train and guide Formulations staff in day-to-day activities.

Skills

Formulations

Leadership

GLP compliance

Documentation

Communication

Training/Mentoring

Time management

Microsoft Office

Education

Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences

Tools

Microsoft Office Suite

Job description

## Supervisor, FormulationsApply: On-site: Scranton, Pennsylvania 18447: Full time: Posted Today: R103200**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 Here*** 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.**What We Offer**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.**Altasciences’ Benefits Package Includes:*** 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.**Altasciences’ Incentive Programs Include:*** Training & Development Programs* Employee Referral Bonus Program