The Engineering and Validation Division of A.N.D Consulting Inc, are seeking engineers and validation specialists to join our core team of excellence driven professionals to fill the following roles that may become available in the upcoming months and year:
EQUIPMENT VALIDATION ENGINEER/SPECIALIST
CLEANING VALIDATION ENGINEER/SPECIALIST
PROCESS VALIDATION ENGINEER/SPECIALIST
TECH TRANSFER/START-UP ENGINEER
Provide technical support to the manufacturing process including troubleshooting, debottlenecking and process optimization in a solid dosage GMP Pharmaceutical Environment.
Candidates need to have strong writing skills, and a high GMP Compliance aptitude.
Work closely with operators and production supervisors to monitor processes.
Work on improvement projects to reduce cost and improve the efficiency of the production process.
Work directly with clients, vendors, management, and technical peers to improve and or develop existing and new products
Develop and improve batch records and SOPs.
Demonstrate ability to solve problems and implement solutions relating to all aspects of work.
Ability to drive projects to consensus and approval.
Professionally represents the company and division. Interacts confidently with clients, contractors, management and peers.
Excellent oral and written communication skills, including effective presentation skills.
Possess effective skills for developing, performing, evaluating, and/or troubleshooting PLCs and control systems (including SCADA, Delta V, and BMS systems) is a plus.
Must be hands-on and field experienced.
Proficient in Microsoft Word, Excel, Power Point and Project.
With a strong knowledge of solid dosage.
BS in Engineering or Life Sciences (Chemical Engineering preferred).
Must be hands on and field experience.
Minimum 3 years industry experience in a GMP manufacturing environment.
This position is based in Durham, NC but you must be willing to travel locally,
nationally or internationally.
The Engineering and Validation Division of A.N.D. Consulting, Inc. provides Consultation Services to Pharmaceutical and Biotech companies within the global market. Our services include:
Master Plan Development
Automation and Control System Qualification
Writing and Execution of Validation Protocols
Quality Assurance Services
We expect our consultants to be professional and get the job done in an effective AND efficient manner with minimal guidance and supervision.
We expect our consultants to excel at their work,
By working hard, being diligent, asking the right questions, meeting project deadlines, and exceeding client expectations.
While being honest, having integrity, taking personal responsibility and having respect for people.