Mechanical Designer in Aiken

Energy Jobline ZR; Aiken (SC); Presencial; USD 65 000 - 90 000; Tempo integral

Resumo da oferta

MR Lowcountry, LLC. in the Aiken, SC area seeks a Mechanical Designer to support 2D/3D designs and documentation for biotech/pharma facilities. You will work under senior engineers to ensure GMP compliance and accurate drawings.

The role emphasizes AutoCAD proficiency, collaboration with process and automation teams, and contributing to projects from concept through installation within a regulated manufacturing setting.

Qualificações

• Associate’s or Bachelor's degree in Mechanical Engineering Technology, Mechanical Design, or related field.
• 2–5 years of mechanical design experience; entry-level with strong/co-op experience considered.
• Proficiency in AutoCAD 2D and AutoCAD 3D; produce complete design packages independently.
• Basic understanding of GMP requirements and design documentation practices in a regulated environment.
• Working knowledge of GD&T, engineering calculations, and material selection.
• Strong attention to detail and ability to manage multiple drawing deliverables.

Responsabilidades

• Develop 2D and 3D mechanical drawings, models, and assemblies using AutoCAD and AutoCAD 3D in GMP/compliant environments.
• Assist in design of process equipment, piping, utilities, and facility modifications for biotech/pharma areas.
• Produce and maintain engineering docs: P&IDs, layouts, BOMs, specs.
• Support design calculations, tolerance analyses, and material selections for cleanrooms.
• Review vendor drawings and verify equipment meets requirements.

Conhecimentos

Attention to detail

GMP awareness

Cross-functional collaboration

Communication skills

Formação académica

Associate's or Bachelor's in Mechanical Engineering Technology or related field

Ferramentas

AutoCAD 2D

AutoCAD 3D

SOLIDWORKS

Inventor

EDMS

Descrição da oferta de emprego

Job DescriptionJob Description

MR Lowcountry, LLC.

Nebo, NC 28761 Telephone: [phone] [e-mail]

Mechanical Designer Aiken, SC area - Full Time-On-Site

Position Summary

The company’s headquarters is in Massachusetts. They produce plant-based ingredients in their manufacturing facility using a variety of patented and proprietary microbial technologies. Our specialty products are in the field of food ingredients, flavors and fragrances, agricultural chemicals, and pharmaceuticals.

The Mechanical Designer supports the design, development, and documentation of mechanical systems, equipment, and facilities used in biotech and pharmaceutical manufacturing environments. Working under the direction of senior engineers and project leads, this role contributes to projects from concept through installation, ensuring designs comply with GMP regulations, FDA guidelines, and applicable industry standards. The ideal candidate brings solid AutoCAD and AutoCAD 3D proficiency, a foundational mechanical background, and an eagerness to grow within a regulated manufacturing setting.

Why work for the Company:

• Opportunity – To be part in building a company focused on a future increasingly reliant on bio-manufacturing and making a sustainable and positive impact in the world.
• Accountability – You will build, manage and work in a hands-on environment to develop and articulate the company’s product value propositions.
• Passion – We love what we do and enjoy working with others who feel the same way. We embrace the challenge and hard work that come with working on bringing cutting edge technologies to market.

Key Responsibilities:

Design & Engineering

• Develop 2D and 3D mechanical drawings, models, and assemblies using AutoCAD and AutoCAD 3D in compliance with GMP and cGMP standards.
• Assist in the design of process equipment, piping systems, utility systems, and facility modifications for biotech/pharma manufacturing areas.
• Produce and maintain engineering documentation including P&IDs, equipment layouts, installation drawings, BOMs, and design specifications.
• Support design calculations, tolerance analyses, and material selections appropriate for cleanroom and regulated environments.
• Review vendor drawings under guidance from senior staff; help verify equipment meets functional and regulatory requirements.

Project Execution

• Support mechanical design workstreams on capital projects from initiation through commissioning and qualification (IQ/OQ).
• Collaborate with process engineers, automation engineers, quality, and facilities to ensure mechanical designs align with operational requirements.
• Assist with equipment procurement activities including RFQ preparation and participation in FATs/SATs.
• Coordinate with contractors and construction teams during installation; provide field support as directed.
• Track design deliverables, manage drawing revisions, and maintain controlled document packages in accordance with change control procedures.

Compliance & Quality

• Ensure all mechanical designs adhere to FDA 21 CFR Part 210/211, ASME BPE, and other relevant standards under guidance from senior staff.
• Participate in design reviews and risk assessments; document findings and follow up on assigned action items.
• Support change control and deviation management processes from an engineering design perspective.
• Maintain drawing and document archives in the company engineering document management system (EDMS).

Collaboration

• Work closely with senior designers and engineers to develop technical skills and understanding of GMP design principles.
• Follow established CAD standards, drawing templates, and best-practice documentation for the engineering team.
• Participate actively in cross-functional project teams and communicate design status to team members and stakeholders.

Qualifications

Required

• Associate’s or Bachelor’s degree in Mechanical Engineering Technology, Mechanical Design, or related field
• 2–5 years of mechanical design experience; entry-level candidates with strong or co-op experience will be considered
• Proficiency in AutoCAD 2D and AutoCAD 3D; ability to produce accurate, complete design packages independently
• Basic understanding of GMP requirements and design documentation practices in a regulated environment
• Working knowledge of GD&T, engineering calculations, and material selection
• Strong attention to detail and ability to manage multiple drawing deliverables concurrently

• Experience in a GMP-regulated biotech or pharmaceutical manufacturing environment
• Familiarity with ASME BPE piping standards and hygienic design principles
• Exposure to cleanroom classifications (ISO 5–8) and HVAC/environmental control concepts
• Experience with SOLIDWORKS or Inventor as a supplemental tool
• Familiarity with engineering document management systems (EDMS)
• Lean / continuous improvement mindset or coursework

Work Environment & Physical Requirements

• Work is performed in a combination of office/CAD environment and active manufacturing/lab areas including cleanrooms.
• Occasional gowning required when entering classified manufacturing spaces; adherence to site EHS and GMP protocols is mandatory.
• May require occasional travel to vendor sites for FATs or to other company facilities.
• Ability to lift up to 25 lbs and stand/walk on the production floor for extended periods during project support activities.

Other Duties

Please note this job description does not fully describe or provide a comprehensive list of all duties and responsibilities of the position. Duties and responsibilities, including essential functions, may vary amongst locations and/or individuals holding this job position, and may be added or changed without notice. All qualified applicants will receive consideration for employment and will not be discriminated against based , , , , , , , , or protected veteran status. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. We are an Equal Opportunity Employer M/F/Vets/.