Manufacturing Process Engineer / Pharma Industry

Our client, a world-leading Pharmaceutical Company in Athens, GA is currently looking for a Manufacturing Process Specialist to join their expanding team.

Position Details : Job Title : Manufacturing Process Specialist / Pharma IndustryDuration : 15 months contract, extendable up to 24 monthsLocation : Athens, GANote : The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.

You may participate in the company group medical insurance planJob Description : Process SpecialistNotes : Role will sit ONSITE in Athens, GAWill be a "backup " to the On-Call personRole is more "Process Specialist "The role is in the API Manufacturing, a Senior RoleBachelors degree requiredMust have exp in API bkgWill help support day-to-day operationsMust have excellent Communication skillsMust have excellent Time Management skillsMust have GMP expWill work with non-performance investigations, document investigations, and help provide corrective actionsWill be working with Manufacturing Supervisors and PlannersShould have Technical Writing expNeed someone who can learn the Science aspect of the jobThis is an Automated Process, should be familiar with those environmentsMust have at least 2 yrs expEssential Job Duties and Responsibilities : The Process Specialist is the technical expert who is responsible for providing technical supportfor 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 correctiveactions 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 andtechnical 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;Minimum Qualification : ;Education : ;High school education / GED plus two years formal technical education / training or;

EquivalentBachelor's degree in science preferred.Experience and Skills : 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 scheduleform.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 trendsPreferred : Experience with SAP and Minitab.

Experience with process control systems (e.g. PCS 7, Emerson DeltaV) and data historiansoftware (e.g. OSi PI).Solid understanding of Word, Power Point, and Excel.

Other Requirements : Regularly required to talk and hear, stand, walk, sit, use tactical sense, handle or feel,and reach with hands and arms.

Required to move around the manufacturing plant to perform on-site investigations.Needs to perform gowning procedures to work in manufacturing core.

Specific vision abilities required by this job include close vision, distance vision, depthperception, and ability to adjust focus.

Off-shift work may be required. On-call support may be required. Must be available for other duties as required.Travel Requirements : up to 10% domestic / internationalNeeds to be mobile and able to independently transport themselves between various sites / locations, as dictated by the essential functions and responsibilities of the position.