Job description
: Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With over 40 years of experience and a growing team of over 2,200 experts servicing global clients from North America and European sites, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing. At Cambrex, our people set us apart. We’re committed to attracting, nurturing, and retaining a passionate and talented team of valued experts in our fast-paced and growing company. We offer an exceptional benefits package including medical, dental, vision, Life, LTD, generous vacation in your first year, sick time, and retirement savings! Known for our scientific and manufacturing excellence, as well as our strong customer focus, we offer a range of career opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Overview:
All employees are required to adhere to DEA, EPA, FDA and cGMP regulations as they relate to the operation of the Company; and to adhere to all company safety rules and procedures. All employees are expected to report to work regularly and promptly. Other duties relating to departmental mission, not specifically detailed in this section may be assigned. Qualifications:
Cambrex is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.
Cambrex Charles City offers an extraordinary opportunity, a competitive salary, and an exceptional benefits package including medical, dental, vision care and prescription, life, LTD, STD; 401(k) with employer match; tuition reimbursement; and the ‘Arthur I. Mendolia Scholarship Program.’ Relocation assistance will be offered for this position.
#CB
The Production Supervisor will be expected to supervise operating personnel for safe, efficient and profitable operation of the chemical manufacturing area. The incumbent will be responsible for administration of day to day manpower, equipment and processing needs of the plant site. The Production Supervisor will work closely with all departments to ensure timely shipment of quality products, meeting or exceeding customer expectations. Shift work required.
Responsibilities:
- Ensuring assigned production area meets or exceeds all safety and quality requirements
- Scheduling operations in a manner that prevents delays and efficiently utilizes manpower
- Ensuring adherence to Standard Operating Procedures in all operations and activities
- Ensure employees are properly trained and evaluate their performance
- Exercising proper care in the utilization of buildings, equipment and services
- Performing simple laboratory tests on samples of in-process and waste materials to ensure proper operation and equipment function
- Coordinating operations with Maintenance Department to complete scheduled and unscheduled maintenance activities for operations area
- Make recommendations to improve yields and reduce waste, labor, materials, maintenance, handling and other costs
- Initiate investigation of production issues and work with support groups to resolve and implement corrective and preventative actions
- Work with Process Engineering and Chemical Development during the implementation of new products in the manufacturing area
- Participate in process evaluations with production superintendents or process engineers as assigned
All employees are required to adhere to DEA, EPA, FDA and cGMP regulations as they relate to the operation of the Company; and to adhere to all company safety rules and procedures. All employees are expected to report to work regularly and promptly. Other duties relating to departmental mission, not specifically detailed in this section may be assigned.
- High School Diploma or equivalent
- Three or more years of chemical processing/manufacturing experience preferred
- Prior supervisory experience beneficial
- Sound written and oral communication skills
- Strong computer knowledge in Windows based software required
- DEA background check required
- Respirator use required
Cambrex is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.
Cambrex Charles City offers an extraordinary opportunity, a competitive salary, and an exceptional benefits package including medical, dental, vision care and prescription, life, LTD, STD; 401(k) with employer match; tuition reimbursement; and the ‘Arthur I. Mendolia Scholarship Program.’ Relocation assistance will be offered for this position.
#CB
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