Salas O'Brien
Founded in 1975, Salas O’Brien is an employee-owned engineering and professional services firm focused on achieving positive impact for our clients, our team, and the world. We know that tomorrow’s requirements are today’s opportunities, and we are here to design lasting solutions for pressing challenges.
We work across a variety of industries providing integrated engineering and consulting services. Our specialized experience includes design for data centers, healthcare, science and technology, high-rise buildings, clean energy, education, and other building types as well as structural and building sciences, infrastructure asset management, advanced robotics, and more.
Hughes Consulting, A Salas O’Brien Co.,
is currently accepting applications for
CQV Engineers
with relevant experience in either facilities, equipment or utilities within a pharmaceutical or biotechnology manufacturing environment to support future projects. Perform Commissioning, Qualification, Validation team activities. Control CQV plan by reviewing documentation, protocols, procedures, and execution strategies, coordinating with vendors and team members. Generate C&Q Procedures. Participate in the development of CQV Planning, ETOP and Documentation Reviews, Protocol Generation and Protocol Execution. Help develop Validation objectives by reviewing project proposals and plans, conferring with management. Prepare validation reports by collecting, analyzing, and summarizing information during execution. Work with startup teams during the commissioning and validation phases of a project, ensuring clear communication and hand-off of information. Maintain a safe and clean working environment by enforcing procedures, rules, and regulations. You will have: Bachelor’s or Master's degree in Engineering or related field (Chemical, Mechanical or equivalent preferred). Minimum 5 years of relevant work experience in Commissioning, Qualification and Validation of Equipment, Utilities or Facilities within a cGMP environment. Strong understanding of commissioning activities. Proficiency in life sciences manufacturing processes in areas such as biotech, aseptic fill/finish, OSD, critical utilities. Knowledge of industry regulated guidelines for the validation of cGMP facilities. Excellent verbal and written communication skills. Technical Documentation Skills. Desired Skills: Ability and willingness to travel. Equal Opportunity Employment Statement Salas O’Brien provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state/provincial, or local laws. Salas O’Brien will accommodate the disability-related needs of applicants as required by law. Seniority level
Associate Employment type
Full-time Job function
Engineering, Manufacturing, and Other Industries
Pharmaceutical Manufacturing, Engineering Services, and Manufacturing
#J-18808-Ljbffr
is currently accepting applications for
CQV Engineers
with relevant experience in either facilities, equipment or utilities within a pharmaceutical or biotechnology manufacturing environment to support future projects. Perform Commissioning, Qualification, Validation team activities. Control CQV plan by reviewing documentation, protocols, procedures, and execution strategies, coordinating with vendors and team members. Generate C&Q Procedures. Participate in the development of CQV Planning, ETOP and Documentation Reviews, Protocol Generation and Protocol Execution. Help develop Validation objectives by reviewing project proposals and plans, conferring with management. Prepare validation reports by collecting, analyzing, and summarizing information during execution. Work with startup teams during the commissioning and validation phases of a project, ensuring clear communication and hand-off of information. Maintain a safe and clean working environment by enforcing procedures, rules, and regulations. You will have: Bachelor’s or Master's degree in Engineering or related field (Chemical, Mechanical or equivalent preferred). Minimum 5 years of relevant work experience in Commissioning, Qualification and Validation of Equipment, Utilities or Facilities within a cGMP environment. Strong understanding of commissioning activities. Proficiency in life sciences manufacturing processes in areas such as biotech, aseptic fill/finish, OSD, critical utilities. Knowledge of industry regulated guidelines for the validation of cGMP facilities. Excellent verbal and written communication skills. Technical Documentation Skills. Desired Skills: Ability and willingness to travel. Equal Opportunity Employment Statement Salas O’Brien provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state/provincial, or local laws. Salas O’Brien will accommodate the disability-related needs of applicants as required by law. Seniority level
Associate Employment type
Full-time Job function
Engineering, Manufacturing, and Other Industries
Pharmaceutical Manufacturing, Engineering Services, and Manufacturing
#J-18808-Ljbffr