Current Career Opportunities

Project Manager – Facilities

Project Manager – Tech. Ops.

Controller

Process Engineer

Process Engineer – Process Development / Technical Transfer

Quality Control Chemist

Quality Control Microbiologist

QC Laboratory Technician

Quality Standards Manager

QA Validation Engineer

Manufacturing/Packaging Technicians

 *************************

Project Manager - Facilities

We are seeking a Facilities Project Manager to lead and coordinate facility, utility, and general infrastructure renovation and construction projects to create safe, compliant, and efficient working environments for the manufacturing, packaging and receiving/distribution of Pharmaceutical solid and liquid dose forms. 

The candidate should possess three or more years of facilities-related project management experience.  Strong technical writing, communication, and computer skills (Microsoft Word, Excel, and Project) are required.  The candidate must be an excellent team leader, and be self-motivated and able to handle multiple priorities.

The candidate must be able to understand and interpret technical drawings.  Strong problem solving skills are required. 

Pharmaceutical manufacturing experience is desired, as are AutoCAD skills and a Bachelor of Science/Bachelor of Engineering degree (engineering related). 

 *************************

Project Manager - Tech. Ops.

We are seeking a seasoned Project Manager who will perform as Project Manager for new business start ups, major business initiatives, and major commercial projects/improvements.  The Project Manager will lead and coordinate the transfer process, and will lead a cross-functional team to bring a new product, equipment, and process into the facility. 

 The candidate must have strong communication skills, strong computer skills (Excel, Word, and Microsoft Project), strong leadership and mechanical skills.  The candidate must have three to seven years of experience in a pharmaceutical manufacturing facility. 

A Bachelor of Science/Bachelor of Engineering (BS/BE) Technical Degree is desires as well as strong technical skills, including technical writing.

 *************************

Controller

We are seeking an accomplished Controller with experience in a multi-customer outsource manufacturing environment. The preferred candidate will hold a CPA designation and have 5-7 years of relevant experience in the outsourcing industry, ideally in a pharmaceutical setting.

Primary skills required for the role include: Financial Reporting, Forecasting, Budgeting & Capital Management, Management Accounting, Purchasing, and Accounts Payable & Receivables.

The Controller position will report to the Vice President, Finance.

The successful candidate will be expected to exhibit a high level of independence in the fulfillment of his/her responsibilities and must possess strong leadership, priority setting, communication, and interpersonal skills that will enable them to successfully manage in a highly participative management work system.

*************************

Logistics Planner

We are seeking a Logistics Planner to be responsible for the translation of Customer Forecasts into Production Plans within a Master Production Schedule. The position is responsible for reviewing inventory levels, schedules, and availability of selected items, either manufactured or purchased. Using MRP, the position is responsible for reviewing and acting on order releases, action, and exception messages from SAP and other systems. This individual is integral in supporting Customer Accounts & ensuring the Customer is satisfied with all aspects of service that Norwich Pharmaceuticals provides.

Key Selection Criteria:

  • Planning experience in a manufacturing setting

  • Strong interpersonal skills

  • Able to manage in a dynamic and changing environment

  • Knowledge of MRPII & SAP computer systems

*************************

Process Engineer

We are seeking an experienced Process Engineer with 3 or more years experience in a Pharmaceutical Manufacturing Facility, strong Process Validation skills, and a Bachelor of Science/Bachelor of Engineering (BS/BE) Technical Degree.

The ideal candidate possesses Process Control skills, Packaging Line knowledge, Drying Technology knowledge, and an ability to communicate with customers.

The candidate must possess an ability to get to root cause and drive solutions and must also demonstrate strong interpersonal skills, strong problem solving skills, and an ability to work in a team environment. Experience with Design of Experiments, process mapping, assessment and improvement is also desired.

 

*************************

Process Engineer - Process Development / Technical Transfer

We are seeking an experienced Process Engineer for our Process Development/Technical Transfer department, who will be responsible for assuring that process start-ups and technical transfers are performed with excellence, delivering robust, compliant, safe, and well-understood processes to be turned over to the Production Business Unit.  

 The Candidate must posses strong Technical Writing Skills, Problem Solving Skills and Mechanical Background.

 Three to seven years of experience in a pharmaceutical manufacturing facility performing technical transfers, start ups, process troubleshooting or formulations is required. 

 A Bachelor of Science/Bachelor of Engineering Technical Degree is desired (prefer Chemistry, Pharmacy, Engineering), as well as process validation experience, strong interpersonal skills, Design of Experiments (DOE) and Statistical Analysis.

*************************

Quality Control Chemists

We are seeking QC Chemists who have a BS in chemistry or related science, plus three to five years of pharmaceutical lab experience, preferably in QC or analytical development.

The candidate must have HPLC experience. Expertise in analytical techniques (Dissolution Testing, UV/Vis, sample preparation, Wet Chemistry, USP/EP raw material testing, spectrographic) is also required.

The candidate must also have experience with Microsoft Excel and Word. The candidate must be a clear communicator and able to execute complex work with minimal oral or written direction. An ability to perform laboratory benchwork in a fast-paced environment is necessary.

The candidate must be able to work second shift (3:00 PM to 1:30 AM Monday through Thursday, and 3:00 PM to 7:00 PM Friday).

 

*************************

Quality Control Microbiologist

Experienced Microbiologist with expertise in microbiology techniques – USP/EP monograph testing of Pharmaceutical Raw Materials, and Finished Product. Main focus to be USP/EP harmonized testing. Experience in validation / prep testing of USP/EP microbiology test methodology.

BS/MS in Microbiology or related science plus 5-10 years directly related pharmaceutical laboratory experience. Excellent oral and written communication skills. Strong team leadership skills. Demonstrated analytical and problem solving skills. Ability to perform laboratory bench work in a fast-paced environment. Proficient in Word and Excel and able to learn new applications.

Capable of working 2nd shift.

*************************

Quality Control Laboratory Technician

Full-time Temporary Role from May 5th, 2008 to August 1, 2008 (13 weeks)

The QC Laboratory Technician performs activities supporting the laboratory function such as reagent and sample inventory control, ordering, filing, record keeping, distribution, and coordination.  Duties typically include administrative functions, chemical handling, or limited laboratory analysis.  Performs work in accordance with established procedures and work systems and suggests system improvements. 

 The QC Lab Technician handles packaged and unpackaged chemicals, removal of expired or depleted stock, and coordinates sample disposal. 

Maintains laboratory apparatus and supplies.

High school diploma, plus 3 years working experience required.  Strong oral and written communication skills.  Proficient with Work and Excel. An ability to learn new software applications.  SAP/MRP system experience desired.  Ability to follow standard operating procedures to perform work function.  Strong clerical aptitude, sound judgment, operates with a sense of urgency in a fast-paced environment.  Strong organizational, communication, and interpersonal skills.

 Multiple priority management skills, efficient time management skills, above average interpersonal skills, problem solving skills.  Customer interface skills, pharmaceutical plant experience desired.

*************************

Quality Standards Manager

Responsibilities include creation and maintenance of raw materials, packaging component, intermediate and finished product specifications. Review USP/NF and EP for changes and manage the implementation of changes. Train and qualify all QA/QC personnel in SAP. Quality Standards SAP. Maintenance of Methods. Maintenance of Quality Assurance Techniques (QATs).

Other responsibilities include: Creation and design of Production records for Manufacturing and Packaging operations. Creation and design of Cleaning records for Manufacturing and Packaging operations. Prioritization of Production record work and communication of prioritization to Logistics. Creation and maintenance of SAP for production records. Write/revise SOPs for Quality Standards. Represent and explain standards systems to customers.

BA/BS/MS in Chemistry. Previous work experience in Quality Standards including a broad range of Pharmaceutical Quality Assurance (plant quality groups and/or systems). Experience in the following areas is desired: Cleaning Validation, Laboratory operations, Production and Packaging operations, SAP design and validation, Packaging laboratory operations, Compliance, and USP & Ph. Eur. testing standards.

*************************

QA Validation Engineer

Primary responsibilities: Perform validation activities in all disciplines of validation (Process, Equipment, Laboratory, Computers, Cleaning, or Facilities) with a specialization in a minimum of two of those disciplines. Prepare, review, and approve validation protocols, reports and compile and analyze validation data. Review and approve validation change controls and make recommendations for corrections to change controls including validation strategies and validation implementation plans. Perform validation assessment of Process, Equipment, Laboratory, Computers, Cleaning, and Facilities systems. Investigate and troubleshoot problems and determine solutions. Maintain appropriate validation documentation and files.

Minimum of 8 years prior experience in a pharmaceutical manufacturing facility involving manufacturing, packaging, quality control, quality assurance, and/or validation.
Knowledge of quality systems, predicate rule, FDA/ICH guidance documents, commonly-used concepts, practices, and procedures. Strong interpersonal skills to work well with diverse groups including customers, management and production technicians. This includes an ability to work in a team environment.
Strong problem solving skills with an ability to get to a root cause.
Strong technical writing skills a must.

BS/BE technical degree desired. Ability to prepare validation protocols, reports compile and analyze validation data and make recommendations for changes and/or improvements to equipment, processes, and systems. Execute validation protocols.
Investigate and troubleshoot problems and determine solutions. Maintain appropriate validations documentation and files.

*************************

Manufacturing/Packaging Technicians

Will participate in the preparation of granulations/blends, compression of tablets, encapsulation of products, coating and inspection of tablets, operation of manual and automated packaging equipment for pharmaceutical products.

Must adhere to standard operating procedures precisely and be well versed in operational details according to strict cGMP standards. Expected to be a fully contributing team member and continually work to enhance technical competence; capable of working independently.

Full-time positions - 3 shifts with availability to work any shift as required. High school education required with strong literacy skills, industrial experience desired (manufacturing or packaging). Must have mechanical aptitude, logical thinking skills and the ability to work in a team environment. Entry salary $12.00/hour with opportunity for significant growth within a five-step pay system, as skills are acquired.


Norwich Pharmaceuticals is an Equal Opportunity Employer.

For any career questions or to send a resume, please e-mail your request to hr@norwichpharma.com

or Send resumes to:

Norwich Pharmaceuticals Inc.
6826 State Highway 12
Norwich, NY 13815
Attn: Human Resources
Fax: 607-335-3007