Job details
Job type full-time
Full job description
: at cambrex, it’s our people that set us apartWe work locally and have an impact globallyWe’re committed to attracting, nurturing and retaining a passionate and talented team of experts in our fast paced and growing companyYou will be valued and recognizedWe offer an exceptional benefits package including medical, dental, vision, life, ltd, generous vacation in your first year, sick time, and retirement savings! cambrex is the small molecule company that provides drug substance, drug product and analytical services across the entire drug lifecycleKnown for our scientific and manufacturing excellence and customer focus, we offer a range of career opportunities across our global network of locationsAs a team, we share one goal – to improve the quality of life for our customers’ patients across the worldOverview: the product manager - generic control substances is the technical liaison with commercial generic controlled substance (cs) customers and coordinates activities for amphetamines, fentanyl, and other identified generic controlled substance productsThis position has frequent interactions with customers, sales representatives, production, quality assurance and regulatory affairs to ensure customer needs are met while maintaining compliance with regulatory requirements and ensuring efficient product manufacturing.
Responsibilities:
Lead or participate in investigation teams as needed when deviations or rejects occur and prepare the report of findings
Provide a high level of customer interaction and technical support
Maintain a high level of positive and effective communication with customers, team members, management and sales representatives
Serve as resource for sales, senior management and customer service regarding allotment and customer feedback
Organize and coordinate multi-disciplinary teams for customer driven initiatives
Coordinate with the production planner to maintain the long term production schedule balancing customer need, efficiency and inventory
Estimate and update product costs as necessary
Monitor compliance with controlled substance manufacturing requirements and provide assistance to regulatory affairs for the purpose of inventory tracking and quota issues
Assist with production management responsibilities for batch record reviews, investigations, and trackwise approvals
All employees are required to adhere to osha, epa, dea, fda and cgmp regulations as they relate to the operation of the company; and to adhere to all company safety rules and proceduresAll employees are expected to report to work regularly and promptlyOther duties relating to departmental mission, not specifically detailed in this section may be assigned.
Qualifications:
A minimum of a bachelor`s degree in chemistry or chemical engineering
5 or more years of experience in a pharmaceutical manufacturing organization
Experience with overall management and responsibility for project teams
Familiarity with cgmp regulations
Direct customer contact and relationship management
General knowledge of chemical operations equipment and manufacturing operations
Skills managing multi-disciplinary teams
Understanding of business plans and financial impacts
Good project management skills requiredHigh attention to detail
Windows based computer knowledge
Remote possibility a couple of days a week - primarily need to onsite.
Generous relocation assistance!!
#1 small molecule api contract manufacturing organization (cmo) in the usa
Double digit sales growth each of the last 5 years
Recent $75 million expansion of our large-scale api facility
Winner of 30 cmo leadership awards in 2017
Iowa – ranked #1 state for best place to live by us news and world report
Leading western supplier of generic apis including adhd and other controlled substances
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.
