Why Join Societal CDMO?

Mission and Culture:

Each day we Bring Science to Society as we work towards improving the quality of life for patients who benefit from the therapies that we manufacture. We strongly believe that every employee plays an impactful role in accomplishing our mission of improving patients’ lives through client partnerships. Whether you are working hands-on in developing, manufacturing, or, testing the products or if you are utilizing your expertise in any other way, through your work here you will have an opportunity to positively affect countless lives.

We foster a culture that is diverse, inclusive, challenging, and supportive. At Societal, we are committed to continuous improvement both as individuals and as an organization. We encourage our employees to continue their personal and professional development in various ways.

Your New Role At Societal:

We are looking for a Supervisor, Manufacturing. In this role, you are responsible for implementing and supervising daily (shift) activities in a specific production area to ensure manufacturing goals, production schedules, and project deadlines are met while maintaining compliance, environment health and safety guidelines and any other regulations that apply.

How You Will Make An Impact:

• Demonstrate the ability and knowledge required to effectively operate production equipment used in area supervised.

• Assist manufacturing management in the daily operation of the department.

• Participate in process investigations, manufacturing equipment qualification, process validation activities, and internal audits of manufacturing area.

• Inspect the manufacturing rooms for cleanliness, neatness, and safety.

• Troubleshoot and notify maintenance/facilities to fix any processing and mechanical problems.

• Order all component inventory supplies (sample bottles, etc.)

• Work together with Material Services on all warehouse issues relating to in-process, raw materials, and finished manufacturing product.

• Submit and/or maintain and distribute reports related to attendance, labor, efficiency, safety, scrap and others as needed.

• Ability to utilize resources and raw materials in the most efficient and productive manner possible.

• Co-ordinate daily processing schedules against the manufacturing schedule (daily drumming checklist, equipment calibration, daily sample sheet, major/minor cleans).

• Ensure batch records are accurate prior to QA review.

• Communicate to and co-ordinate manufacturing activities with the Process Controller, Manufacturing Management, and Manufacturing Planner.

• Monitor security of controlled substances during all phases of transport and processing performed by manufacturing employees and ensure appropriate documentation is completed.

• Maintain a safe work area and monitor Manufacturing Associates to ensure adherence to all SOPs, Safety and Company policies.

• Regular and reliable attendance on a full-time basis.

• Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.

• Embodies Societal’s cultural values and aligns daily actions with department and company culture

Ideal Candidate Will Bring:

• Generally, Four (4) years of experience with solid oral dose pharmaceutical manufacturing with a bachelor’s degree or High School diploma with six (6) years of experience.

• Generally, a minimum of one (1)  years of experience leading and managing teams.

Benefits:

At Societal, we offer a diverse and competitive total rewards package to attract and retain talent. In addition to base compensation, all employees are eligible for one of our annual performance opportunities (bonus or commission). In addition, we offer a wide range of benefits including medical, dental, vision, paid time off, paid company shutdowns and holidays, 401k matching, life insurance, paid parental leave and much more.

Who is Societal:

Societal is a bi-coastal contract development and manufacturing organization (CDMO) with expertise to deliver on our client’s needs, regardless of complexity level. These projects span pre-Investigational New Drug (IND) development to commercial manufacturing and packaging for a wide range of therapeutic dosage forms. We provide industry-leading support for small molecule therapeutic development, end-to-end regulatory support, clinical and commercial manufacturing, aseptic fill/finish, lyophilization, packaging, and logistics services to the global pharmaceutical market. We do all of this in our best-in-class facilities in San Diego, California, and Gainesville, GA.

New hires will pass a background check and drug screen as a condition of employment.

We are an EOE dedicated to a diverse workforce and a Drug-Free work environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other characteristic protected by law. If you require an accommodation to complete the application or interview process, please contact careers@societalcdmo.com.Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. 41 CFR 60-1.35(c)