Share Email Opening Title Process Development Technician II  Category Research & Development   Description Why Join Recro: Mission and Culture: Our leadership proactively works to create and foster a culture that exemplifies our core values and mission. We strive to provide a work environment that is diverse, inclusive, challenging, and supportive. We are committed to continuous improvement both as individuals and as an organization and encourage our employees to continue their personal and professional development in a variety of ways. We strongly believe that every employee plays a crucial role in accomplishing our mission of improving patients’ lives through client partnerships. Whether you are working hands on developing, producing 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. 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: We are looking for a Process Development Technician II. In this role you will operate process development (PD) equipment and will be responsible for manufacturing of research and clinical products. You will conduct routine monitoring of PD suite and equipment and take inventory of PD materials and supplies. You will assist in writing standard operating procedures, protocols, batch records and development reports. How You Will Make An Impact: Weighing, dispensing, and keeping manual inventory of raw materials, in-process materials and finished product. Setting up, operating and cleaning equipment in Product Development such as Wurster fluid-bed processors, rotor granulators, tablet presses, Fitzmills, V-blenders, hard gelatin encapsulation machines, or capsule checkweighers. Perform sampling and physical testing of research in-process materials, e.g. sieve analysis, particle size analysis, loss-on-drying, microscopy, etc. Completing written documentation of work performed such as logbook entries, batch records, and material tracking forms. Maintaining cleanliness of PD suite including mopping, disposing of garbage and general housekeeping duties. Conducting physical inventories for controlled/non-controlled substances. Routine monitoring of facilities and equipment, such as magnehelic gauges, water systems and stability chambers. Assist in execution of IOQs for processing equipment. Assist in training manufacturing operators for new product transfers.   Position Requirements Ideal Candidate Will Bring: Minimum education of a High School diploma. Minimum of 5 years’ experience in related pharmaceutical manufacturing environment utilizing a wide verity of manufacturing equipment, including 2 years’ experience in solid oral dosage manufacturing. Working knowledge of cGMP regulations and safety procedures. Ability to work effectively in a team environment and to lead and train junior staff members. Ability to solve mathematical problems that require multiple operations, simple ratios, factions, percentages and perform unit conversions. Ability to read and comprehend written instructions with good communication skills. Occasionally lift and/or move up to 25 pounds, frequently lift and/or move up to 50 pounds, and occasionally lift and/or move more than 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Must have corrected visual acuity of 20/40 or better bilaterally. Must be able to pass color/contrast testing passing 9 of 12 elements. Must be able to pass a Pulmonary Function Test (PFT) and wear appropriate Personal Protection Equipment such as a respirator.   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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