Share Email Opening Title Manufacturing Associate I -2nd Shift  Category Manufacturing   Description 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 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 and we encourage our employees to continue their personal and professional development in a variety of ways. Benefits: We offer a competitive total rewards package that includes health benefits, annual performance bonus, stock options, generous paid time off, holiday shutdowns, parental leave, matching 401k contributions, and much more! Your New Role At Societal: We are looking for a Manufacturing Associate I. This position is a 2nd shift position. Hours are 3:00 PM - 11:30 PM Monday Through Friday. The 2nd shift will have an additional 10% shift differential added to the base salary. n this role, you will perform critical manufacturing activities in a GMP environment. You will follow Standard Operating Procedures (SOPs) and Batch Record Instructions to complete manufacturing and validation processes, set up, clean, and maintenance of a variety of manufacturing equipment; and document activities as they occur. How You Will Make An Impact: Learn to execute instructions included in batch records to manufacture a variety of pharmaceutical products in accordance with Standard Operating Procedures and cGMP guidelines. Learn to set up, operate, clean, and perform basic maintenance of equipment used in the manufacturing processes. Learn to troubleshoot and repair manufacturing equipment with Facilities guidance and support. Support validation activities for new equipment and processes by performing activities outlined in validation protocols and with guidance from Engineers or Supervisors. Document all activities completed either in batch records, equipment logs, check sheets, or another format as required per procedures. Coordinate with Manufacturing Management to schedule sample preparation and submission to QC on products manufactured. Performs material management activities - weigh, stage, and load materials; package final product; account for material used, lost in production processes, and/or returned to inventory. Document deviations and out-of-specification (OOS) or out-of-tolerance (OOT) results. Participate in continuous improvement efforts for the department   Position Requirements Ideal Candidate Will Bring: HS diploma or General Education Degree (GED is required.  Technical education or associate’s degree in a relevant field would be a plus. No prior work experience is required, but six (6) months of experience working in a cGMP manufacturing environment is highly preferred.  Mechanical aptitude to be able to understand the setup and operation of automated and semi-automated equipment. Good organizational and prioritization skills with strong attention to detail Effective written and oral communication skills with the ability to comprehend written instructions and procedures. Ability to operate personal computers with a general understanding of MS Office programs (Word, Excel, Access, Outlook). Basic knowledge of safety procedures applicable to a manufacturing environment Exposure to continuous improvement tools - 6S Lean, brainstorming, value mapping, 5 Why's, etc.    Ability to add, subtract, multiply and divide in all units of measurement, using whole numbers, common fractions, and decimals.  Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. Who is Societal: Societal, previously Recro, 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. If you would like to apply for this position, please visit our website at www.recrocdmo.com and click on the "Careers" section. New hires will pass a background check, drug screen, and will be required to show proof of COVID vaccination (subject to limited qualified exemptions) as a condition of employment. We are an equal opportunity employer (EOE) dedicated to a diverse workforce and 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.   About the Organization 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, Georgia. New hires will pass a background check and drug screen as a condition of employment.   EOE Statement 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.   EmpID None Specified  This position is currently not accepting applications. To search for an open position, please go to http://Societal.appone.com WE ALSO RECOMMEND Other Jobs Within Same Category -- None found -- Other Jobs Within 60 Miles -- None found --

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