Formulation Specialist I Pilot Facility
Formulation Specialist I Pilot Facility
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Salary Not Disclosed
1 Vacancy
Job Description
States considered: Michigan
Role Description
POSITION SUMMARY
The Pilot Facility (PF) Formulation Specialist supports the Oral Solid Dose (OSD) Pilot Facility by preparing assembling operating and cleaning manufacturing equipment for animal health products. This role demands meticulous attention to detail adaptability to new processes adherence to manufacturing standards and strong communication and teamwork skills.
POSITION RESPONSIBILITIES
- Support Pilot Facility small scale batch production.
- Ability to understand and operate all manufacturing equipment in PF. Become proficient in blending and weigh/dispense tableting granulation roller compaction and all associated equipment
- Operate maintain troubleshoot and make minor repairs on Pilot Facility equipment
- Work with Project leaders by participating in batch planning manufacture and follow up. Effectively communicate issues regarding process materials and personnel to the Project leader or Pilot Facility Director.
- Set up batch equipment and supplies for manufacture
- Clean rooms and equipment and leave ready for next manufacture in appropriate state of cleanliness
- Become proficient at tablet and powder inprocess test equipment such as Tap Density LOD Disinegration Hardness Friability Mass Flow etc.
- Review completed batch records to ensure correctness compliance with GMPs etc. Work with team to correct errors and on batch record structure/content for improvement/error reduction.
- Scan and organize batch records for on and offline access
- Participate in Project team meetings SOP revision Continuous improvement for the area and projects etc
- Train new specialists
- Ensure all tasks are performed in accordance with applicable batch records standard operating procedures (SOPs) and safety guidelines as well as applicable regulatory standards such as current Good Manufacturing Practices (cGMPs)
- Assembly disassembly and proper cleaning of Pilot Facility equipment and work areas
- Ability to train on area SOPs/OJTs equipment process paperwork.
- Capable of collecting and assembling data for review.
- Ability to work with hazardous materials in a controlled manner by following proper gowning procedures all SOPs and safety guidelines
- Follow specific and detailed recipe instructions requiring right first time measuring and mixing of ingredients to create finished products
- Monitor evaluate and adjust processes or equipment to maximize quality and efficiency
- Maintain complete and accurate documentation of all tasks completed
- Effectively communicate with Project leaders support personnel and area leadership
TECHNICAL SKILLS REQUIREMENTS
- Knowledge of cGMPs and production practices
- Experience in a Lean Production and/or manufacturing environment
- Reliable transportation and good attendance/time management skills
- Experience in Lean Manufacturing and continuous improvement work environment; 5S visual schedule PDCA M1 etc.
- Ability to train on area SOPs/OJTs equipment process paperwork
- Experience in working with Tech Writer creating and maintaining training documentation
EDUCATION AND EXPERIENCE
- High school diploma or general education degree (GED)
- Basic math and legible writing reading comprehension
- 25 years of relevant pharmaceutical or packaging experience
- Demonstrated Mechanical reasoning and troubleshooting skills
- Ability to follow detailed instructions
- Effective interpersonal communication and a positive outlook
- Mechanical reasoning and troubleshooting skills
- Knowledge of cGMPs and production practices
- Computer Skills: Microsoft Applications preferred
- Individual must be selfmotivated and be able to work independently
- Good oral and written communication skills
PHYSICAL REQUIREMENTS
The work characteristics described here are representative of those a colleague encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job the colleague is regularly exposed to a manufacturing environment including moving mechanical parts. The work conditions for this position are 100 standing and walking throughout the workday and require routing lifting of 2050lbs. The colleague will be required to utilize certain Personal Protective Equipment including but not limited to hard hats safety (steeltoed) shoes eye protection gloves PAPRs and protective clothing. Manual dexterity and ability to keep up with pace of production standards.
Work Environment: Colleague will work in a facility that manufactures Cephalosporins and must not be Cephalosporin sensitive. Must work near moving mechanical parts. Flexible hours and overtime may be required.
Full timeRegularColleagueAny unsolicited resumes sent to Zoetis from a third party such as an Agency recruiter including unsolicited resumes sent to a Zoetis mailing address fax machine or email address directly to Zoetis employees or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.
Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race color religion sex sexual orientation age gender identity or gender expression national origin disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at to request an accommodation. Zoetis also complies with all applicable national state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: 1 our company website at site or 2 via email to/from addresses using only the Zoetis domain of @zoetis. In addition Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.Required Experience:
Unclear Seniority
Employment Type
Full-Time
