Manufacturing Technician - Weekend shift

abbvieKansas City, MO13 days ago

Occupations

Production Workers, All Other Chemical Equipment Operators and Tenders Mixing and Blending Machine Setters, Operators, and Tenders

Industries

Pharmaceutical Preparation Manufacturing Biological Product (except Diagnostic) Manufacturing Research and Development in Biotechnology (except Nanobiotechnology)

Job TitleCarry out daily tasks as assigned by the Production Manager according to GMP and the quality system. Active involvement and management of batch related CAPA's as they arise in the business unit taking them from the initial review state through RCA, approval, batch disposition and delivery of corrective and preventive actions, liaising closely with the relevant Departments and QA Lead to ensure thorough investigation is completed and timely resolution and closure is met. Accurately completing documentation in a timely manner, accurately and legibly. Responsible for maintaining & monitoring grade A conditions inside isolator, including end of batch EM and utilizing the FMS system for data collection and completing glove testing for integrity of RAB units. Adhering to all company standards in safety, housekeeping and quality, notifying management of any discrepancies. Competent in surface sanitization and use of qualified Disinfectants/Detergents/Biocide cleans, competent in both SIP sterilization & bespoke autoclave counter pressure training. Manage requirements in order to deliver the KPIs as they relate to the Product Flow function with a specific emphasis on the 32 day release cycle Follow gowning procedures on entry to areas and donning additional garbing for specific tasks within the compounding area. Adhere to and support all EHS & E standards, procedures, and policies.

Qualifications:

Understanding of the requirements to work in a regulated GMP industry
Ability to build strong relationships and work within cross-functional teams.
Adaptability to work in a fast, dynamic environment whilst adjusting readily to meet unexpected constraints.
Drive, high energy, maturity, and ability to work under pressure, deliver results, and overcome obstacles.
Team player who can collaborate with others to achieve organizational targets and goals.
Knowledge of biologics operations an advantage
Excellent communication skills
Ability to use sound judgment to make effective decisions within appropriate timeframes
Proven to be self-directed, self-motivated and ability to prioritize competing priorities
Excellent technical writing skills is a requirement for this role and previous experience on GTW i.e. opening RCC's / LIRs / CAPA's is preferrable in order to be successful within this role 2-3 Years working in a manufacturing environment, preferably Aseptic/Sterile Manufacturing.
Experience working in a cleanroom environment.
Third Level qualification in science or engineering discipline is an advantage but not essential.

Additional Information: AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/ Fraud AlertWe have recently become aware of various recruitment phishing scams targeting job seekers. Please be advised: AbbVie will never request sensitive personal information (such as bank account details, social security numbers, or payment of any kind) during the recruitment process. If you suspect you have received a fraudulent offer or communication claiming to be from AbbVie, please do not respond, open any attachments, or click on any hyperlinks. If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us yourself by verifying job offers and communications. Your safety is important to us. Where We WorkRole is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.

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Level

JuniorL3

Location

Kansas City, MO

Occupation

Production Workers, All Other

Industry

Pharmaceutical Preparation Manufacturing

Posted

13 days ago

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