Job Description:

• The Process Specialist is the technical expert who is responsible for providing technical support

• for the Active Pharmaceutical Ingredient (API), medical device raw material or medical device component manufacturing processes under limited direction of operations management. These responsibilities include providing technical expertise to ensure that atypical event and nonconformance investigations relating to production are completed in compliance with all applicable procedures and regulations, monitors and trends key process parameters, troubleshoots manufacturing problems as required and identifies and implements process improvements, supports capital projects, site wide initiatives or other projects as needed in the capacity of a project lead or a subject matter expert and conducts technical and validation studies.

• Provides primary (on floor) production support.

• Plan, prepare, issue, and control production schedule and material requirements to ensure control flow of approved material timed to meet production plan.

• Facilitate the implementation of the production plan.

• Takes corrective action for daily operational problems within the department.

• Act as subject matter expert (SME), providing guidance on deviations, investigations, and issues pertaining to quality of product.

• Study the need for improvements of existing processes, systems and equipment, and in cooperation with related departments, undertakes optimization to increase efficiency and quality and to reduce costs.

• Recommends and implements corrective/preventative measures aimed at improving compliance and reducing repeat occurrences. Follow up to determine if corrective

• actions adequately addressed root cause of NC event.

• Provides technical support for the investigation and resolution of deviations and atypical events by partnering with Quality Assurance to ensure consistent quality standards are maintained.

• Tracks deviations, events and key process parameters and provides reports to management on trending, and status as requested. Recommends corrective actions for

• any trends identified.

• Identifies and implements process improvements related to safety, environmental, quality, compliance, productivity, yield, and cost. Assure regulatory compliance and

• technical feasibility of proposed changes.

• Initiate and execute change controls for projects.

• Retrieve and use data to monitor process performance and proactively troubleshoot; operations. Work with Automation and Information Management to improve the; effectiveness of process data collection and analysis.;

• Ensure department quality and safety compliance.;

• Plan and direct the administration and implementation of assigned projects as required; for the manufacture of the company's products.;

• Live Our Credo and Purpose by putting the need of Our Credo; stakeholders first, pursuing the highest standards of compliance, quality and ethics.

• Connect inclusively within the department, with other departments, and within the; company to address customer needs.;

• Shape the future through innovation by inspiring new ideas, trying new things, and; demonstrating resilience and agility to adapt to change.;

• Grow by developing self and others to reach goals by engaging in open and honest; conversations, managing energy, and taking ownership for outcomes.; Additional position requirements:;

• Provide documentation support for SOP/ Batch Record revisions.;

• Identify necessary document changes and ensure timely revision to all SOP and batch; records.;

• Review and approve SOP and batch record revisions.;

• Assist with equipment startup and technical training as required.;

• Provide technical support for process and cleaning validation maintenance and; verification. Assist with cleaning cycle optimization and revalidation efforts.;

• Demonstrates expertise in the following areas: cGMPs, FDA regulations, manufacturing; processes, manufacturing equipment, high purity water systems, and utilities.;

• Responsible for handling controlled substances in compliance with applicable State and; local law and requirement.;

• Supervisory responsibilities;

• None;

Responsibilities:

• Generally, 4-6 years of work experience in a chemical, pharmaceutical, medical device or similarly regulated manufacturing industry.

• Ability to learn and operate SAP Production, COMET, SUMMIT, to the level required.

• Technical understanding of at least one processing area.

• Ability to read, analyze and interpret procedure manuals, common scientific and technical journals, basic financial reports and legal documents, general business periodicals and government regulations.

• Ability to respond to sensitive inquiries and present information to Site Management, regulatory agencies and members of the business community.

• Ability to define problems, collect relevant data and information, establish facts, and draw valid conclusions as required.

• Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.

• Demonstrated ability to write effectively to communicate work prepared, rationalize conclusions and recommendations, and compliantly document for regulatory bodies.

• Manage and coordinate multiple project priorities as required.

• Ability to work independently on routine and non-routine tasks.

• •Successfully completes regulatory and job training requirements.

• Remains current in skills and industry trends

Experience:

• Role is more "Process Specialist"

• The role is in the API Manufacturing, a Senior Role

• Will help support day-to-day operations

• Must have excellent Communication skills

• Must have excellent Time Management skills

• Must have GMP exp

• Will work with non-performance investigations, document investigations, and help provide corrective actions

• Will be working with Manufacturing Supervisors and Planners

• Should have Technical Writing exp

• Need someone who can learn the Science aspect of the job

• This is an Automated Process, should be familiar with those environments

• Must have at least 2 yrs exp

Preferred:

• Experience with SAP and Minitab.

• Experience with process control systems (e.g. PCS 7, Emerson DeltaV) and data historian software (e.g. OSi PI).

• Solid understanding of Word, Power Point, and Excel.

Skills:

• Must have exp in API bkg

Education:

• Bachelors Required

About US Tech Solutions:

US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com (http://www.ustechsolutionsinc.com) .

US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,

national origin, disability, or status as a protected veteran.