REMOTE Marketing & Commercial Excellence Manager- EAST COAST

Cambrex
Remote or New Jersey
At Cambrex, it's our people that set us apart. We work locally and have an impact globally. We're committed to attracting, nurturing and retaining a passionate and talented team of experts in our fast paced and growing company. You will be valued and recognized. We 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 lifecycle. Known for our scientific and manufacturing excellence and customer focus, we offer a range of career opportunities across our global network of locations. As a team, we share one goal - to improve the quality of life for our customers' patients across the world.

The Marketing & Commercial Excellence Manager's primary purpose is to ensure that the overall marketing & commercial strategy for Cambrex and all its business units (BUs), is accurately executed in marketing activities and delivers on the marketing generated funnel, driving the overall growth of new customer acquisitions. Reporting into the Senior Director of Marketing & Communications, this role will provide leadership, strategic direction, and divisional oversight for the specific BU marketing functions by generating customer demand and loyalty through the deployment of a clear and compelling marketing strategy, marketing campaigns and marketing operations activities. The one key goal is to understand and interpret the market and industry trends, build, and execute the marketing activities to drive lead generation and awareness expansion for the BUs.
Responsibilities

* Develop and implement growth marketing strategies and plans to increase brand awareness for Cambrex in a specific BU market and create lead generation to meet revenue targets for the specific BU
* Assess and understand the competition's value to our target customer base & strategic accounts
* Define value propositions based on the intersection of the needs of the customer, target audience, the value the business provides, and the gaps in the competitive landscape
* Responsible for planning and implementing commercial insight activities, gather competitive intelligence, actively monitor changes to the market, provide regular updates on market intelligence, design pro-active plans to capture opportunities and address hurdles in close relationship with the internal market intelligence team and external consultants
* Responsible for category management for the BUs in different sub-segments, including game theory development, value proposition, strategy, marketing position etc.
* Work closely with the commercial team and SMEs for content development to support the marketing communication plan, including white paper, webinars, videos, solution content, videos, articles, website content, etc. Content needs to reflect the different BU dimensions.
* In co-ordination with the Sales team, implement a lead generation process to generate leads, nurture leads and opportunities and drive conversion to sales
* Analyze results of marketing programs and modify strategies to support business objectives and continuously improve the marketing activities

Qualifications

* 5 or more years experience preferably in an industrial and B2B marketing
* Experience in chemical, drugs/small molecule industry, preferred
* Bachelors degree in Business, Marketing, communications or similar, preferred
* Digital marketing experience including SEO, required
* Passionate and outgoing, with strong communication and teamwork skills
* Experience in using Salesforce, Pardot, Tableau, HubSpot and other similar platforms

Sr. Computer System Validation Engineer

Cambrex
Remote or Durham, NC
At Cambrex, it's our people that set us apart. We work locally and have an impact globally. We're committed to attracting, nurturing and retaining a passionate and talented team of experts in our fast paced and growing company. You will be valued and recognized. We offer an exceptional benefits package including medical, dental, vision, Life, STD, 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 lifecycle. Known for our scientific and manufacturing excellence and customer focus, we offer a range of career opportunities across our global network of locations. As a team, we share one goal - to improve the quality of life for our customers' patients across the world.

Cambrex (www.Cambrex.com) is seeking a highly motivated, energetic, results-oriented individual to join our team of dedicated professionals focused on customer service and quality. This role will be responsible for managing and executing GxP CSV projects from project kickoff through system go-live. Project will range in size from simple off the shelf systems to large enterprise systems.

This is primarily a remote position that will require periodic onsite visits to support projects activities. Onsite support is estimated to be once a month but will be dependent on project requirements and schedule.
Responsibilities

* Works closely with project stakeholders (IT, System Owner, QA) to effectively and efficiently implement new systems, system upgrades, or system modifications
* Develops and manages project schedules to drive efficient projects executions
* Manages consultants to ensure that project timeline, budget, and quality are maintained
* Manages CSV projects under a GAMP lifecycle framework
* Writes, reviews, approves and executes all system lifecycle documents (URS, Validation Plan, Specifications, Risk Assessment, Qualifications IQ/OQ/PQ, Data Integrity Evaluations, Trace Matrix, SOP's, Validation Summary Report)
* Conducts data integrity evaluations and enforces the required data integrity controls
* Supports client and regulatory audit activities
* Assist in development, implementation, and enforcement of computer system validation and data integrity policies and practices

Qualifications

* At least 5 years of experience managing and executing Computer System Validation projects in a GAMP framework
* At least 3 years of project management experience
* Strong understanding of 21CFR Part 11 and Data Governance/Data Integrity requirements
* Strong experience with technical writing, risk assessment, gap analysis, change control and deviation management
* BS/BA

Technical Proposal Writer - Remote

Cambrex
Remote or Longmont, CO
At Cambrex, it's our people that set us apart. We work locally and have an impact globally. We're committed to attracting, nurturing and retaining a passionate and talented team of experts in our fast paced and growing company. You will be valued and recognized. We offer an exceptional benefits package including medical, dental, vision, Life, STD, 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 lifecycle. Known for our scientific and manufacturing excellence and customer focus, we offer a range of career opportunities across our global network of locations. As a team, we share one goal - to improve the quality of life for our customers' patients across the world.

The Technical Proposal Writer is responsible for writing and pricing technical proposals for multiple services, primarily supporting formulation development and drug product manufacturing, but also assisting with analytical chemistry, process chemistry and drug substance manufacturing as possible. The Technical Proposal Writer will act as the primary contact with Business Development, the technical team, Project Management, Finance and Legal to support proposal preparation and facilitate the onboarding and execution of the projects from a business perspective.
Responsibilities

* Responsible for writing high quality proposals for various service offerings, specifically in support of Formulation Development for Early Stage Development.
* Interact with Business Development (BD) team and external customers on Requests for Proposals (RFPs)
* Coordinate with BD to schedule Subject Matter Expert (SME) meetings for RFP reviews
* Responsible for working with key stakeholders (SMEs, Project Managers, etc.) to clearly define project scope, strategy, resource requirements, timelines, deliverables and pricing
* Preparation of detailed project proposals, including supporting materials such as cost workbooks and high-level Gantt charts

* Participate in peer review of proposals to support Business Operations team
* Maintain accurate and timely updates to Salesforce.com in support of forecasting activities
* Support Project Accounting in revenue and invoicing activities as needed
* Work closely with BD to achieve budget, optimize profit, and fill the schedule
* Engage in development of new approaches, procedures, and processes in Business Operations

Qualifications

* Bachelor's Degree or higher in Pharmaceutical Sciences, Chemistry, or closely related field
* 5+ years of early stage development work experience
* Early stage formulation development experience, desired
* Experience writing highly technical research-based proposals
* Knowledge of early stage CDMO market pricing and conditions useful
* Experience with Service Agreements useful
* Proficiency with the entire MS Office suite
* Preferred proficiency with Salesforce.com or similar CRM tool

SUCCESS FACTORS:

* Formulation development and/or drug product manufacturing expertise
* Ability to write highly technical proposals
* Strong business acumen and problem-solving skills
* Excellent planning and organizational skills
* Ability to work in a fast-paced, cross-functional team
* Superior verbal and written communication skills with both internal and external customers
* Effective negotiating skills

Senior Technical Proposal Writer - Remote

Cambrex
Remote or Longmont, CO
At Cambrex, it's our people that set us apart. We work locally and have an impact globally. We're committed to attracting, nurturing and retaining a passionate and talented team of experts in our fast paced and growing company. You will be valued and recognized. We offer an exceptional benefits package including medical, dental, vision, Life, STD, 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 lifecycle. Known for our scientific and manufacturing excellence and customer focus, we offer a range of career opportunities across our global network of locations. As a team, we share one goal - to improve the quality of life for our customers' patients across the world.

The Sr. Technical Proposal Writer is responsible for writing, pricing, and reviewing technical proposals for multiple early stage development services, primarily supporting drug substance and drug product development, including GMP manufacturing and associated analytical and quality activities. The Sr. Technical Proposal Writer will act as the primary contact with Business Development, the technical team, Project Management, Finance and Legal to support proposal preparation, including participation in development strategy and related planning activities.
Responsibilities

* Responsible for writing high quality proposals for various service offerings, specifically in support of Early Stage Development, including GMP manufacturing (drug substance and/or drug product)
* Interact with Business Development (BD) team and external customers on Requests for Proposals (RFPs)
* Coordinate with BD to schedule Subject Matter Expert (SME) meetings for RFP reviews
* Responsible for working with key stakeholders (SMEs, Project Managers, etc.) to clearly define project scope, strategy, resource requirements, timelines, deliverables and pricing
* Preparation of detailed project proposals, including supporting materials such as cost workbooks and high-level Gantt charts

* Participate in peer review of proposals to support Business Operations team
* Maintain accurate and timely updates to Salesforce.com in support of forecasting activities
* Support Project Accounting in revenue and invoicing activities as needed
* Work closely with BD to achieve budget, optimize profit, and fill the schedule
* Participate in development of new approaches, procedures, and processes in Business Operations
* Participate in business growth strategies and pricing discussions

Qualifications

* Bachelor's Degree or higher in Chemistry or closely related field
* 7+ years of early stage development work experience
* GMP manufacturing work experience is desired
* Experience writing highly technical research-based proposals
* Knowledge of early stage CDMO market pricing and conditions useful
* Proven experience in strategic pricing and planning
* Experience with Service Agreements useful
* Proficiency with the entire MS Office suite
* Preferred proficiency with Salesforce.com or similar CRM tool

SUCCESS FACTORS:

* Drug substance/drug product manufacturing expertise
* Ability to write highly technical proposals
* Strong business acumen and problem-solving skills
* Excellent planning and organizational skills
* Ability to work in a fast-paced, cross-functional team
* Superior verbal and written communication skills with both internal and external customers
* Effective negotiating skills

REMOTE Business Development Director- West Coast

Cambrex
Remote or Longmont, CO
At Cambrex, it's our people that set us apart. We work locally and have an impact globally. We're committed to attracting, nurturing and retaining a passionate and talented team of experts in our fast paced and growing company. You will be valued and recognized. We offer an exceptional benefits package including medical, dental, vision, Life, STD, 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 lifecycle. Known for our scientific and manufacturing excellence and customer focus, we offer a range of career opportunities across our global network of locations. As a team, we share one goal - to improve the quality of life for our customers' patients across the world.

Cambrex is looking for an ambitious and energetic Business Development Director to grow our Drug Substance/API CDMO business. The primary function of this role is to aggressively grow pipeline, prospects but most importantly revenues by identifying and securing new accounts for the company. The role also includes identifying new business opportunities from the existing accounts. The right candidate will enjoy working in a team environment to help to help grow the entire Cambrex portfolio.
Responsibilities

The responsibilities of the Business Development / Sales Professional will include, but not be limited to the following:

* Aggressively pursue Drug Substance/API CDMO business opportunities, via prospecting, building strong client relationships, forging new business partnerships, nurturing and qualifying leads, and maintaining high visibility within networking and trade organizations within the defined territory.
* Identify industry and customer needs and actively contribute to provide solutions that will generate value for the customer.
* Be an important part in the ongoing liaison between groups internal to Cambrex and the external customer.
* Lead the initiative to introduce new projects and business opportunities pursuant to Cambrex´s overall business strategy both at existing and new accounts.

Qualifications

EDUCATION:

* Minimum of a Bachelor's degree in Chemistry or related life-science degree is required.

EXPERIENCE:

* A minimum of 3-5 years experience in business development, with proven track record in selling Drug Substance/API CDMO services. Some experience in CMC services, drug product and finishes dose form, fine chemicals, and custom technologies is desired. Commercial experience in pharmaceutical or related industry is preferred.

The successful candidate for this position will have the following:

* Entrepreneurial disposition, energetic and takes personal responsibility in accomplishing the objectives of the business.
* Strong "hunting" skills
* The ability to inspire customer confidence, promote and develop strong client to business relationships and become the provider of choice for existing and new clients.
* The ability to effectively engage in discussions with procurement, technical, chemical and pharmaceutical scientists in order to generate business opportunities.
* The ability to handle multiple customers (Effective time management, good organization skills effective use of resources and assessment of priorities to opportunities).
* Strong relationship building skills across disciplines (technical, commercial and management).
* Excellent verbal and written communication skills (The ability to communicate internally and externally to the organization with the credibility necessary to influence sales and customer decisions).
* An understanding of cGMP manufacturing requirements as well as regulatory and environmental issues relevant for the pharmaceutical industry.
* A solid team player who can maintain cohesiveness between the customer, R&D and Manufacturing. Also comfortable in a project centered organization.
* The ability to work effectively within a multicultural environment.
* A high level of energy, creativity and personal motivation.
* The determination and persistence to build a business.

Senior QC Scientist

Cambrex
Longmont, CO
At Cambrex, it's our people that set us apart. We work locally and have an impact globally. We're committed to attracting, nurturing and retaining a passionate and talented team of experts in our fast paced and growing company. You will be valued and recognized. We offer an exceptional benefits package including medical, dental, vision, Life, STD, 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 lifecycle. Known for our scientific and manufacturing excellence and customer focus, we offer a range of career opportunities across our global network of locations. As a team, we share one goal - to improve the quality of life for our customers' patients across the world.

As Analytical (QC) Scientist, you will execute analytical methods and provide general analytical support, such as release and stability testing of drug substances and drug products.
Responsibilities

* You will execute analytical methods for in-process control, release testing and stability monitoring of bulk drug substances and drug products under cGMP guidelines.
* You will develop and implement test methods utilizing U/HPLC, GC, NMR, HPLC/MS, dissolution, IR and/or various analytical techniques.
* You will write standard operating procedures (SOPs), method qualification/validation protocols and reports (GMP/GLP), and research study reports .
* As Analytical Scientist, you will follow SOPs and clearly documents all procedures and results in a GMP notebook.

Qualifications

* BS Degree or MS Degree in Chemistry or related discipline plus a minimum of 3-5+ years of industrial experience in a GMP environment is required.
* Experience in chromatography and wet analytical chemistry is required.
* A strong understanding of advanced analytical techniques (i.e. NMR, HPLC/MS) is preferred.
* Method development and validation experience with drug substance and drug product is preferred.
* Excellent customer service and communication skills are required.
* Ability to write reports and business correspondences.
* Ability to listen and respond well to external customers, partners and colleagues at all levels.
* Prioritizes tasks according to business objectives and can pursue several objectives simultaneously.

Associate Scientist - Analytical

Cambrex
Longmont, CO
At Cambrex, it's our people that set us apart. We work locally and have an impact globally. We're committed to attracting, nurturing and retaining a passionate and talented team of experts in our fast paced and growing company. You will be valued and recognized. We offer an exceptional benefits package including medical, dental, vision, Life, STD, 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 lifecycle. Known for our scientific and manufacturing excellence and customer focus, we offer a range of career opportunities across our global network of locations. As a team, we share one goal - to improve the quality of life for our customers' patients across the world.

As Analytical Research Scientist, you will execute analytical methods and provide general analytical support, such as release and stability testing of drug substances and drug products.
Responsibilities

* You will execute analytical methods for in-process control, release testing and stability monitoring of bulk drug substances and drug products under cGMP guidelines.
* You will develop and implement test methods utilizing U/HPLC, GC, NMR, HPLC/MS, dissolution, IR and/or various analytical techniques.
* You will write standard operating procedures (SOPs), method qualification/validation protocols and reports (GMP/GLP), and research study reports .
* As Analytical Scientist, you will follow SOPs and clearly documents all procedures and results in a GMP notebook.

Qualifications

* BS Degree or MS Degree in Chemistry or related discipline plus a minimum of 2+ years of industrial experience in a GMP environment is required.
* Experience in chromatography and wet analytical chemistry is required.
* A good understanding of advanced analytical techniques (i.e. NMR, HPLC/MS) is preferred.
* Method development and validation experience with drug substance and drug product is preferred.
* Good customer service and communication skills are required.
* Ability to write reports and business correspondences.
* Ability to listen and respond well to external customers, partners and colleagues at all levels.
* Prioritizes tasks according to business objectives and can pursue several objectives simultaneously.

Manufacturing Quality Assurance Specialist

Cambrex
Longmont, CO
At Cambrex, it's our people that set us apart. We work locally and have an impact globally. We're committed to attracting, nurturing and retaining a passionate and talented team of experts in our fast paced and growing company. You will be valued and recognized. We offer an exceptional benefits package including medical, dental, vision, Life, STD, 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 lifecycle. Known for our scientific and manufacturing excellence and customer focus, we offer a range of career opportunities across our global network of locations. As a team, we share one goal - to improve the quality of life for our customers' patients across the world.

The Manufacturing Quality Assurance Specialist is responsible for manufacturing operations support. This position will work directly with manufacturing, analytical, and other departments to ensure that products conform to quality standards and all applicable regulatory requirements.
Responsibilities

* Provide Quality support for manufacturing operations.
* Responsible for batch record issuance and review.
* Coordinate and facilitate Deviations, Change Controls, CAPAs and OOS events as related to manufacturing operations.
* Review and approve validation protocols for manufacturing related equipment, facilities, and utilities.
* Review and approve calibration and maintenance events.
* Support the Quality team to achieve quality goals and metrics.
* Communicate effectively with internal personnel, as well as external customers.

Qualifications

* BS or BA Degree with 2-5+ years, MS Degree with 2+ years, working in a Biotech or Pharmaceutical FDA regulated industry.
* Prior experience in a manufacturing quality assurance support role, preferably in oral solid dosage and drug substance manufacturing.
* Prior experience maintaining pharmaceutical quality systems.
* Experience, or understanding, with international guidance and their application to early to late stage pharmaceutical programs.
* Experience with and working knowledge of cGMP and GLP quality systems, policies, and regulations/guidelines.
* Ability to influence others for the better of the company.
* Participate in developing department goals, objectives, and systems.
* Exceptional analytical and problem-solving skills with the proven ability to think strategically.
* Highly effective team and interpersonal skills with the ability to work across numerous scientific and management disciplines.
* Ability to influence employees in a matrix organization to ensure completion to pre-established due dates.

Operational Excellence Manager

Cambrex
Longmont, CO
At Cambrex, it's our people that set us apart. We work locally and have an impact globally. We're committed to attracting, nurturing and retaining a passionate and talented team of experts in our fast paced and growing company. You will be valued and recognized. We offer an exceptional benefits package including medical, dental, vision, Life, STD, 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 lifecycle. Known for our scientific and manufacturing excellence and customer focus, we offer a range of career opportunities across our global network of locations. As a team, we share one goal - to improve the quality of life for our customers' patients across the world.

The Operations Excellence Manager coordinates with a variety of business units to develop, test and refine business processes and practices to provide the site and business unit with a competitive advantage within a pharmaceutical CDMO environment. This role must be able to engage with all levels of technology operation teams, engineering, business process owners and management to innovate and implement processes to support business growth. The goal is to maximize value through efficient systems and freeing up manager's time to focus on the business.

This role is responsible for site-wide process design, using data and metrics to drive continuous improvement and optimization efforts by reducing waste and inefficiencies, but must coordinate efforts across sites within the business unit.
Responsibilities

* Designs and implements changes to processes that improve results and reduce cost and eliminate waste.
* Coordinates with a variety of business units to develop, test, and refine business processes / practices.
* Leverages data to drive continuous improvement in areas such as productivity, quality, customer service, and sales.
* Teaches lessons learned and key findings to departments with recommendations for changes and updates for training.
* Creates a roadmap for tools and technology needed to ensure improvement in processes.
* Proactively address problem areas and improve efficiencies.
* Streamlines processed to allow for expansion

Qualifications

* Minimally a bachelor's degree in a quantitative field from a four-year college or university strongly preferred; and 3+ years related experience within a pharmaceutical and/or CDMO industry.
* Six Sigma/Lean experience a plus.
* Familiar with the design of SOPs, Work Instructions, and Job Aides to improve workflow and compliance
* Knowledge of pharmaceutical manufacturing and laboratory processes
* Understanding of overall stability processes
* Enhance Sample Lifecycle management
* Strong quantitative capabilities. Adept at drawing conclusions from a variety of data sources.
* Successful management of cross-functional teams to perform process analysis, improvement and implementation on a national scope.
* Exceptional analytical, creative, technical project management and interpersonal skills, along with an intense customer focus.
* Tactful communication (written and presentation) style; need to have the ability to create a story and value proposition, develop presentations, and present in front of internal/external clients, as well as frontline to executive levels.
* Experience leading by influence, and success in being a driver of change in an organization.
* Demonstrated ability to think creatively, deal with ambiguity, and manage changing priorities.
* Highly goal and result oriented.
* Prioritizes tasks according to business objectives and can pursue several objectives simultaneously.
* Can work independently with a high degree of self-motivation.
* Knows how to obtain support from different collaborations.
* Tackles problems with enthusiasm and curiosity.
* Treats colleagues at all levels with respect.
* Very effective listening skills with the ability to hear attentively and process information correctly.
* Ability to discuss and reach an agreement in a professional manner.
* Ability to manage and analyze a situation and develop a professional solution to the organization
* Ability to train others

Research Scientist, Process Chemistry

Cambrex
Longmont, CO
At Cambrex, it's our people that set us apart. We work locally and have an impact globally. We're committed to attracting, nurturing and retaining a passionate and talented team of experts in our fast paced and growing company. You will be valued and recognized. We offer an exceptional benefits package including medical, dental, vision, Life, STD, 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 lifecycle. Known for our scientific and manufacturing excellence and customer focus, we offer a range of career opportunities across our global network of locations. As a team, we share one goal - to improve the quality of life for our customers' patients across the world.

Cambrex in Longmont Colorado is seeking a Research Scientist for our process chemistry research group. This position requires expertise in synthetic organic chemistry as well as the analytical instrumentation used in this field (for ex. NMR, HPLC, GC, FTIR). The process chemistry group conducts research into new synthetic routes and optimizes existing processes for the generation of the active pharmaceutical ingredient (API) in developmental drugs for clinical evaluation.
Responsibilities

As a Research Scientist in our Process Research and Development Group, you will:

* Devise new synthetic routes and optimize existing processes for the cGMP manufacture of Active Pharmaceutical Ingredients (APIs).
* Execute laboratory-scale synthetic operations and solve process chemistry issues with sound, innovative strategies.
* Be able to efficiently navigate the current literature through online platforms to solve complex chemistry issues.
* Generate non-GMP demonstration batches of APIs and transfer processes to our manufacturing group.
* Conduct thermal hazard assessment of materials and reactions in a process using DSC, EasyMax and ARC.
* Lead scientific research projects and / or mentor other scientists.
* Conduct and document process optimization studies [for e.g., design of experiments (DoE) and quality by design (QbD)] and apply changes to the modified route.
* Maintain a current and accurate laboratory notebook that documents all experimental results.
* Comply with all safety, health, and environmental requirements.

Qualifications

* Degree Requirements:
* Ph.D., Organic Chemistry with 0-6 years of experience in the pharmaceutical development industry
* M.S., Organic Chemistry with 4-10 years of experience in the pharmaceutical development industry
* B.S., Chemistry with 10+ years of experience in the pharmaceutical development industry

* Ability to effectively set priorities on projects and efficiently manage time to meet contract goals.
* Team player that works well within the process chemistry group but also interacts smoothly with other departments (Analytical Chemistry, Materials Characterization, Pharmaceutics, Quality Management and Manufacturing).
* Good oral and written communication skills for internal meetings and customer meetings/teleconference calls to provide project updates and reports.

Senior QC Scientist

Cambrex
Longmont, CO

Senior Director, Pharmaceutics & Formulation

Cambrex
Longmont, CO

Supervisor Material Management

Cambrex
Longmont, CO

Associate Scientist

Cambrex
Longmont, CO

Process Engineer II

Cambrex
Homestead, IA

Process Safety Engineer

Cambrex
Homestead, IA

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